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Lichtenstein cave Y-DNA markers
Felix Schilz published in the year 2006 his PhD thesis Molekulargenetische Verwandtschaftsanalysen
am Praehistorischen Skelettkollektiv der Lichtensteinhoehle. (Goetinngen 2006).
The full text of the article (pdf format) is here.
In this work were presented values of STR markers obtained for 19 skeleton remnants of male individuals.
These values are here compared with Y-DNA profiles from Databases od the Czech and Slovak Y-DNA.
At Genebáze, it is the second (March 2008) comparison of Y-DNA markers of persons dead before 3000 years.
Lichtenstein cave is situated West of small town Osterode (South of Hannover), Germany.
Acquired Y-STR haplotypes
Total of 19 males were tested and by 16 of them 6 different haplotypes weve observed. They are denoted Y1 till Y6:
the table si taken from the cited thesis
What are the Lichtenstein cave discoveries telling us ?
Until the recent time the genetic genealogy could use only the results acquired from living individuals to examine male lines (the chromozome Y).
Depending on how the particular haplogroups and their subdivisions are spread nowadays it can be presumed, where they were occuring before, where the
migration routes lead and so on. However, the methods of isolating DNA from bones improved so much in the last few years that it enabled in several
cases to determine the Y-STR markers´ values even for individuals deceased a long time ago. The Lichtenstein cave remainders are immensely
interesting for us since they originate from the central Europe and give us data about a small sample of a population of 3000 years ago. So what do
these results tell us ?
1.
There were 19 males among the discovered skeletons and 16 of them could be used for analyzing the Y-STR markers´ values. Among the
individuals some haplotypes occured several times and indicated their pertaining to the same paternal clan. A haplogroup of individuals could be
estimated on the basis of a haplotype. In the 12 cases it was the l1b2 haplogroup (3 different paternal clans), in two cases the
R1a haplogroup (1 paternal clan) and in one case the R1b haplogroup was estimated.
2.
Such a high frequency of the haplogroup I1b2 in this particular area in the time of 3000 years ago is rather unexpected. We would more likely
expect a higher representation of the R1b haplogroup. The I1b2 haplogroup is not entirely strange in the central Europe, though, only
its high representation among the individuals from the Lichtenstein cave is quite unusual. Today, this haplogroup can be found all over the Europe,
but the frequency of this occurrence is somewhere around few percent. Comparatively the greatest number of it is in Germany (and the most of it
particularly in the Niedersachsen, where the Lichtenstein cave is located!), Netherlands, Belgium, England and Scandinavia. It is being considered
that it has arisen somewhere in Germany or northern Italy several thousands years ago.
3.
An occurrence of the R1a in the Lichtenstein cave 3000 years ago is immensely interesting for it demonstrates that the R1a
haplogroup did not come to the central Europe for the first time with the Slavic, but that a particular (small ?) amount of it was here already
before. Naturally, it would be very interesting to try to distinguish this R1a from that one, which came later on with the Slavonic
expansion, but at the current level of knowledge of this haplogroup we are not able to do it so far.
4.
As for the only haplotype connectable to the R1b haplogroup, one can say only that it is very close to the modal (most frequent)
haplotype of this haplogroup and that in its value DYS390=23 it could indicate its clasification to the subgroup R1b1c9.
But this is only a higher level of probability, not the certainty. In any case, this haplotype is a representative of a R1b population,
which can be found most often nowadays in the western Europe.
5.
If someone would find a genetic distance of his haplotype 0-2 from the afore-said individuals from the Lichtenstein cave, he can take it
as an affirmation of a fact that people relative to his paternal line existed in the area of the present Germany in the time of 3000 years ago.
From the hereinafter-mentioned tables it can be seen that the users of our databases have a correspondence with the Lichtenstein cave records
only in the case of the R1b haplogroup. In the rest of haplotypes the best correspondence is at genetic distance 2. In this case a better
correspondence does not mean a closer relationship, though. We are comparing living persons with those deceased 3000 years ago. A haplotype
of their prospective descendants could naturally changed after all this time. To determine a speed of the STR markers´ mutation is a great
problem which probably will not be solved in a short time.
An interesting result of the comparison is that only the Slovak database users have haplotypes close to I1b2 haplotypes of the
inhabitants from the Lichtenstein cave.
Individual profiles and theirs comparison, matches and genetic distances with users
of Czech and Slovak Y-DNA database.
Haplotype Y1
ID |
db |
dys19 |
dys389-1 |
dys389-2 |
dys390 |
dys391 |
dys392 |
dys393 |
dys385a |
dys385b |
dys437 |
dys438 |
dys439 |
Match |
Haplogroup |
genetic distance |
Y1 |
lc |
16 |
12 |
28 |
25 |
11 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
- |
I1b2* (Hapest) |
- |
Y6 |
lc |
16 |
12 |
28 |
24 |
11 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
11/12 |
I2b2* (Hapest) |
1 |
Y2 |
lc |
15 |
12 |
27 |
25 |
11 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
10/12 |
I1b2* (Hapest) |
2 |
I1b2* modal |
Ysearch |
17 |
12 |
28 |
25 |
11 |
11 |
13 |
13 |
16 |
15 |
10 |
11 |
10/12 |
I1b2* modal |
2 |
M1273 |
sk |
16 |
12 |
28 |
23 |
13 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
10/12 |
I1b2* (Hapest) |
4 |
J1634 |
sk |
16 |
12 |
28 |
23 |
10 |
11 |
14 |
13 |
17 |
15 |
10 |
11 |
9/12 |
I1b2* (Hapest) |
4 |
Haplotype Y2
ID |
db |
dys19 |
dys389-1 |
dys389-2 |
dys390 |
dys391 |
dys392 |
dys393 |
dys385a |
dys385b |
dys437 |
dys438 |
dys439 |
Match |
Haplogroup |
genetic distance |
Y2 |
lc |
15 |
12 |
27 |
25 |
11 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
- |
I1b2* (Hapest) |
- |
Y1 |
lc |
16 |
12 |
28 |
25 |
11 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
10/12 |
I1b2* (Hapest) |
2 |
Y6 |
lc |
16 |
12 |
28 |
24 |
11 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
9/12 |
I2b2* (Hapest) |
3 |
I1b2* modal |
Ysearch |
17 |
12 |
28 |
25 |
11 |
11 |
13 |
13 |
16 |
15 |
10 |
11 |
9/12 |
I1b2* modal |
4 |
M1273 |
sk |
16 |
12 |
28 |
23 |
13 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
8/12 |
I1b2* (Hapest) |
6 |
J1634 |
sk |
16
| 12 |
28 |
23 |
10 |
11 |
14 |
13 |
17 |
15 |
10 |
11 |
7/12 |
I1b2* (Hapest) |
6 |
Haplotype Y6
ID |
db |
dys19 |
dys389-1 |
dys389-2 |
dys390 |
dys391 |
dys392 |
dys393 |
dys385a |
dys385b |
dys437 |
dys438 |
dys439 |
Match |
Haplogroup |
genetic distance |
Y6 |
lc |
16 |
12 |
28 |
24 |
11 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
- |
I2b2* (Hapest) |
- |
Y1 |
lc |
16 |
12 |
28 |
25 |
11 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
11/12 |
I1b2* (Hapest) |
1 |
Y2 |
lc |
15 |
12 |
27 |
25 |
11 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
9/12 |
I1b2* (Hapest) |
3 |
I1b2* modal |
Ysearch |
17 |
12 |
28 |
25 |
11 |
11 |
13 |
13 |
16 |
15 |
10 |
11 |
9/12 |
I1b2* modal |
3 |
M1273 |
sk |
16 |
12 |
28 |
23 |
13 |
11 |
13 |
13 |
17 |
15 |
10 |
11 |
10/12 |
I1b2* (Hapest) |
3 |
J1634 |
sk |
16 |
12 |
28 |
23 |
10 |
11 |
14 |
13 |
17 |
15 |
10 |
11 |
9/12 |
I1b2* (Hapest) |
3 |
Haplotype Y3
ID |
db |
dys19 |
dys389-1 |
dys389-2 |
dys390 |
dys391 |
dys392 |
dys393 |
dys385a |
dys385b |
dys437 |
dys438 |
dys439 |
Match |
Haplogroup |
genetic distance |
Y3 |
lc |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
11 |
14 |
15 |
12 |
12 |
- |
R1b (Hapest) |
- |
E1701 |
cz |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
11 |
14 |
15 |
12 |
12 |
12/12 |
R1b (Hapest) |
0 |
K1142 |
cz |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
11 |
14 |
15 |
12 |
12 |
12/12 |
R1b (Hapest) |
0 |
L1538 |
cz |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
11 |
14 |
15 |
12 |
12 |
12/12 |
R1b (Hapest) |
0 |
K1114 |
cz |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
11 |
14 |
- |
- |
12 |
10/10 |
R1b1 (FTDNA) |
0 |
R1b1c9* modal |
Ysearch |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
11 |
14 |
15 |
12 |
12 |
12/12 |
R1b1c9* modal |
0 |
R1b1c* modal |
Ysearch |
14 |
13 |
29 |
24 |
11 |
13 |
13 |
11 |
14 |
15 |
12 |
12 |
11/12 |
R1b1c* modal |
1 |
I1942 |
sk |
14 |
13 |
29 |
24 |
11 |
13 |
13 |
11 |
14 |
15 |
12 |
12 |
11/12 |
R1b (Hapest) |
1 |
E1437 |
cz |
14 |
13 |
29 |
22 |
11 |
13 |
13 |
11 |
14 |
15 |
12 |
12 |
11/12 |
R1b (Hapest) |
1 |
I1931 |
cz |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
11 |
13 |
- |
- |
12 |
9/10 |
R1b (FTDNA) |
1 |
J1253 |
cz |
14 |
13 |
28 |
23 |
11 |
13 |
13 |
11 |
14 |
- |
- |
11 |
9/10 |
R1b (FTDNA) |
1 |
J1370 |
cz |
14 |
13 |
28 |
23 |
11 |
13 |
13 |
11 |
14 |
- |
- |
12 |
9/10 |
R1b (Hapest) |
1 |
K1963 |
cz |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
12 |
14 |
15 |
12 |
12 |
11/12 |
R1b (Hapest) |
1 |
K1826 |
sk |
14 |
13 |
29 |
24 |
11 |
13 |
12 |
11 |
14 |
15 |
12 |
12 |
10/12 |
R1b (Hapest) |
2 |
E1048 |
cz |
14 |
13 |
29 |
23 |
11 |
13 |
14 |
11 |
14 |
15 |
12 |
12 |
10/12 |
R1b (Hapest) |
2 |
E1156 |
cz |
14 |
13 |
30 |
23 |
11 |
13 |
13 |
11 |
14 |
15 |
12 |
13 |
10/12 |
R1b (Hapest) |
2 |
E1336 |
cz |
14 |
13 |
29 |
23 |
11 |
13 |
13 |
12 |
14 |
15 |
12 |
13 |
10/12 |
R1b (Hapest) |
2 |
J1639 |
cz |
14 |
13 |
29 |
24 |
11 |
13 |
12 |
11 |
14 |
15 |
12 |
12 |
10/12 |
R1b (Hapest) |
2 |
J1233 |
cz |
14 |
13 |
29 |
24 |
11 |
13 |
12 |
11 |
14 |
- |
- |
12 |
8/10 |
R1b (GGProj) |
2 |
J1356 |
cz |
14 |
13 |
30 |
23 |
11 |
13 |
13 |
11 |
14 |
- |
- |
11 |
8/10 |
R1b (FTDNA) |
2 |
M1027 |
cz |
14 |
13 |
29 |
24 |
11 |
13 |
13 |
11 |
14 |
15 |
11 |
12 |
10/12 |
R1b (Hapest) |
2 |
E0815 |
cz |
14 |
13 |
29 |
24 |
10 |
13 |
13 |
11 |
15 |
15 |
12 |
12 |
9/12 |
R1b (Hapest) |
3 |
K1382 |
cz |
14 |
14 |
31 |
23 |
11 |
13 |
13 |
11 |
14 |
- |
- |
12 |
7/10 |
R1b1 (FTDNA) |
3 |
M1033 |
cz |
14 |
13 |
30 |
22 |
11 |
13 |
13 |
11 |
13 |
15 |
12 |
12 |
9/12 |
R1b (Hapest) |
3 |
M1383 |
cz |
14 |
13 |
29 |
24 |
11 |
13 |
13 |
12 |
14 |
15 |
12 |
11 |
9/12 |
R1b (Hapest) |
3 |
H1314 |
sk |
14 |
13 |
29 |
24 |
11 |
14 |
13 |
12 |
14 |
15 |
12 |
11 |
8/12 |
R1b (Hapest) |
4 |
E1606 |
cz |
14 |
13 |
30 |
24 |
11 |
13 |
12 |
11 |
14 |
14 |
12 |
12 |
8/12 |
R1b (Hapest) |
4 |
K1335 |
cz |
14 |
13 |
30 |
24 |
11 |
13 |
12 |
11 |
14 |
- |
- |
11 |
6/10 |
R1b (FTDNA) |
4 |
J1962 |
cz |
14 |
13 |
29 |
24 |
10 |
13 |
13 |
12 |
15 |
15 |
- |
12 |
7/11 |
R1b (Hapest) |
4 |
K1630 |
cz |
14 |
13 |
30 |
24 |
11 |
13 |
12 |
11 |
14 |
14 |
12 |
12 |
8/12 |
R1b (Hapest) |
4 |
K1102 |
cz |
14 |
13 |
28 |
23 |
11 |
12 |
13 |
11 |
15 |
15 |
12 |
11 |
8/12 |
R1b (Hapest) |
4 |
M1383 |
cz |
14 |
13 |
29 |
23 |
11 |
14 |
14 |
12 |
14 |
15 |
12 |
11 |
8/12 |
R1b (Hapest) |
4 |
E1448 |
cz |
14 |
14 |
30 |
24 |
11 |
13 |
13 |
11 |
14 |
14 |
11 |
12 |
7/12 |
R1b (Hapest) |
5 |
G0637 |
cz |
15 |
13 |
29 |
24 |
10 |
13 |
12 |
11 |
14 |
15 |
12 |
13 |
7/12 |
R1b (Hapest) |
5 |
L1411 |
cz |
14 |
14 |
30 |
24 |
11 |
13 |
14 |
11 |
14 |
15 |
12 |
11 |
6/12 |
R1b (Hapest) |
6 |
Haplotype Y5
ID |
db |
dys19 |
dys389-1 |
dys389-2 |
dys390 |
dys391 |
dys392 |
dys393 |
dys385a |
dys385b |
dys437 |
dys438 |
dys439 |
Match |
Haplogroup |
genetic distance |
Y5 |
lc |
15 |
13 |
30 |
25 |
11 |
11 |
13 |
11 |
13 |
14 |
11 |
11 |
- |
R1a (Hapest) |
- |
R1a1* modal |
Ysearch |
15 |
13 |
30 |
25 |
11 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
10/12 |
R1a1* modal |
2 |
E1145 |
cz |
16 |
13 |
30 |
25 |
11 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
10/12 |
R1a (Hapest) |
2 |
K1445 |
cz |
15 |
13 |
30 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
10/12 |
R1a (Hapest) |
2 |
R1a* modal |
Ysearch |
16 |
13 |
30 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
9/12 |
R1a* modal |
3 |
H1246 |
sk |
15 |
13 |
29 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
9/12 |
R1a (Hapest) |
3 |
J1634 |
sk |
15 |
13 |
30 |
25 |
11 |
11 |
13 |
11 |
13 |
14 |
11 |
11 |
9/12 |
R1a (Hapest) |
3 |
E0748 |
cz |
15 |
13 |
30 |
24 |
10 |
11 |
13 |
11 |
14 |
- |
- |
11 |
7/10 |
R1a (Hapest) |
3 |
E1325 |
cz |
16 |
13 |
39 |
25 |
11 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
9/12 |
R1a (FTDNA) |
3 |
E1426 |
cz |
14 |
13 |
30 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
9/12 |
R1a (Hapest) |
3 |
H1235 |
cz |
15 |
13 |
29 |
25 |
10 |
11 |
13 |
11 |
14 |
- |
- |
11 |
7/10 |
R1a1 (FTDNA) |
3 |
I1920 |
cz |
16 |
13 |
30 |
25 |
10 |
11 |
13 |
11 |
14 |
- |
- |
11 |
7/10 |
R1a (GGProj) |
3 |
I2168 |
cz |
15 |
14 |
30 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
9/12 |
R1a (FTDNA) |
3 |
K1024 |
cz |
15 |
13 |
30 |
25 |
10 |
11 |
13 |
11 |
14 |
- |
- |
10 |
7/10 |
R1a1 (GGProj) |
3 |
K1692 |
cz |
15 |
13 |
29 |
25 |
11 |
11 |
13 |
11 |
14 |
14 |
- |
10 |
8/11 |
R1a (FTDNA) |
3 |
L1747 |
cz |
15 |
13 |
30 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
9/12 |
R1a (Hapest) |
3 |
L1519 |
cz |
16 |
13 |
30 |
24 |
11 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
9/12 |
R1a (Hapest) |
3 |
H1224 |
sk |
16 |
13 |
30 |
25 |
10 |
11 |
13 |
10 |
14 |
14 |
11 |
11 |
8/12 |
R1a (Hapest) |
4 |
M1178 |
sk |
16 |
14 |
30 |
25 |
11 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
8/12 |
R1a (Hapest) |
4 |
D1549 |
cz |
15 |
13 |
29 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
8/12 |
R1a (Hapest) |
4 |
E1459 |
cz |
16 |
13 |
29 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
8/12 |
R1a (FTDNA) |
4 |
E1639 |
cz |
16 |
13 |
29 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
- |
11 |
7/11 |
R1a (FTDNA) |
4 |
I1909 |
cz |
15 |
14 |
31 |
25 |
11 |
11 |
13 |
11 |
14 |
- |
- |
10 |
6/10 |
R1a (FTDNA) |
4 |
I1953 |
cz |
16 |
13 |
29 |
25 |
10 |
11 |
13 |
11 |
14 |
- |
- |
11 |
6/10 |
R1a1 (FTDNA) |
4 |
J1012 |
cz |
16 |
13 |
29 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
- |
11 |
7/11 |
R1a* (FTDNA) |
4 |
K1687 |
cz |
16 |
13 |
30 |
26 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
8/12 |
R1a (Hapest) |
4 |
K1743 |
cz |
16 |
13 |
30 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
8/12 |
R1a (Hapest) |
4 |
K1136 |
cz |
16 |
13 |
30 |
24 |
11 |
11 |
13 |
11 |
14 |
14 |
11 |
11 |
8/12 |
R1a (Hapest) |
4 |
L1777 |
cz |
16 |
13 |
30 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
8/12 |
R1a (Hapest) |
4 |
M1391 |
cz |
16 |
13 |
31 |
25 |
11 |
11 |
13 |
11 |
14 |
14 |
- |
10 |
7/11 |
R1a (FTDNA) |
4 |
H1359 |
sk |
17 |
13 |
30 |
25 |
11 |
11 |
13 |
10 |
14 |
14 |
11 |
10 |
8/12 |
R1a (Hapest) |
5 |
L1787 |
sk |
16 |
14 |
30 |
25 |
11 |
11 |
13 |
10 |
14 |
14 |
11 |
10 |
7/12 |
R1a (Hapest) |
5 |
E0837 |
cz |
16 |
14 |
30 |
24 |
10 |
11 |
13 |
11 |
14 |
14 |
- |
11 |
6/11 |
R1a1 (FTDNA) |
5 |
E1617 |
cz |
15 |
13 |
29 |
26 |
10 |
11 |
13 |
11 |
14 |
15 |
11 |
11 |
7/12 |
R1a (Hapest) |
5 |
H1036 |
cz |
15 |
13 |
31 |
26 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
7/12 |
R1a (Hapest) |
5 |
H1202 |
cz |
16 |
13 |
31 |
25 |
10 |
11 |
13 |
10 |
14 |
14 |
11 |
11 |
7/12 |
R1a (FTDNA) |
5 |
I2146 |
cz |
16 |
13 |
30 |
26 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
7/12 |
R1a (Hapest) |
5 |
K1381 |
cz |
15 |
13 |
29 |
26 |
10 |
11 |
13 |
11 |
14 |
15 |
11 |
11 |
7/12 |
R1a (Hapest) |
5 |
L1963 |
sk |
17 |
13 |
29 |
25 |
10 |
11 |
13 |
10 |
14 |
14 |
11 |
11 |
7/12 |
R1a (Hapest) |
6 |
A1358 |
cz |
17 |
13 |
30 |
25 |
10 |
11 |
13 |
10 |
14 |
14 |
11 |
10 |
7/12 |
R1a (Hapest) |
6 |
A1632 |
cz |
16 |
14 |
31 |
25 |
11 |
11 |
14 |
11 |
14 |
14 |
11 |
10 |
6/12 |
R1a (Hapest) |
6 |
C1245 |
cz |
16 |
14 |
31 |
26 |
11 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
6/12 |
R1a (Hapest) |
6 |
H1325 |
cz |
16 |
14 |
31 |
25 |
10 |
11 |
13 |
11 |
14 |
14 |
11 |
10 |
6/12 |
R1a (Hapest) |
6 |
Processed 08.04.2008
Jiří Pavlíček, Ludvík Urban
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