I2b*-A
[old
I1b2]
| This subclade is uncommon: based on the database at SMGF, only
about 0.5% of European Hg I are I2b. Geographically widespread in
western Europe, from Iberia, France, and Italy to Germany and Denmark,
but absent from Sweden and Norway. |
| Surname |
Kit
# |
Ysearch
User ID |
SNP
Tests |
Haplotype—
as determined by STR testing |
Known
Lineage |
| Markers 1-12 |
Markers 13-25 |
Markers 26-37 |
Markers 38-67 |
3
9
3 |
3
9
0 |
19
/
3
9
4 |
3
9
1 |
a
|
3
8
5 |
b
|
3
8
5 |
4
2
6 |
3
8
8 |
4
3
9 |
i
|
3
8
9 |
3
9
2 |
ii
|
3
8
9 |
4
5
8 |
a
|
4
5
9 |
b
|
4
5
9 |
4
5
5 |
4
5
4 |
4
4
7 |
4
3
7 |
4
4
8 |
4
4
9 |
a
|
4
6
4 |
b
|
4
6
4 |
c
|
4
6
4 |
d
|
4
6
4 |
4
6
0 |
H4
|
G
A
T
A |
IIa
|
Y
C
A |
IIb
|
Y
C
A |
4
5
6 |
6
0
7 |
5
7
6 |
5
7
0 |
a
|
C
D
Y |
b
|
C
D
Y |
4
4
2 |
4
3
8 |
5
3
1 |
5
7
8 |
a
|
S1
3
9
5 |
b
|
S1
3
9
5 |
5
9
0 |
5
3
7 |
6
4
1 |
4
7
2 |
S1
4
0
6 |
5
1
1 |
4
2
5 |
a
|
4
1
3 |
b
|
4
1
3 |
5
5
7 |
5
9
4 |
4
3
6 |
4
9
0 |
5
3
4 |
4
5
0 |
4
4
4 |
4
8
1 |
5
2
0 |
4
4
6 |
6
1
7 |
5
6
8 |
4
8
7 |
5
7
2 |
6
4
0 |
4
9
2 |
5
6
5 |
| I2b*-A modal values |
13 |
25 |
16 |
11 |
16 |
13 |
11 |
13 |
11 |
12 |
11 |
28 |
16 |
8 |
10 |
10 |
12 |
24 |
15 |
19 |
28 |
14 |
14 |
15 |
15 |
10 |
9 |
19 |
19 |
14 |
14 |
|
|
|
|
11 |
10 |
11 |
8 |
15 |
16 |
8 |
11 |
10 |
8 |
11 |
9 |
12 |
21 |
22 |
|
11 |
12 |
12 |
16 |
8 |
13 |
23 |
21 |
11 |
13 |
12 |
14 |
11 |
12 |
12 |
11 |
Defining markers highlighted in yellow and boldfaced. |
| |
|
|
|
|
|
|
|
|
| STRAUP |
26031 |
E3BJM |
Basic |
13 |
25 |
17 |
10 |
13 |
16 |
11 |
13 |
11 |
12 |
11 |
30 |
16 |
8 |
10 |
9 |
12 |
23 |
15 |
19 |
28 |
14 |
14 |
15 |
15 |
10 |
9 |
19 |
19 |
14 |
14 |
18 |
17 |
34 |
42 |
13 |
10 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pvt7, Earl Frank6,
William
E.5, James
F. STRAUP4,
Thomas3,
David2,
Theobald/Dewald
STRAUB1 — of Carbon Co., PA |
| STROUP |
58687 |
|
Deep |
13 |
25 |
17 |
10 |
13 |
16 |
11 |
13 |
11 |
12 |
11 |
30 |
16 |
8 |
10 |
9 |
12 |
24 |
15 |
19 |
28 |
14 |
14 |
15 |
15 |
10 |
9 |
19 |
19 |
14 |
14 |
18 |
17 |
34 |
41 |
13 |
10 |
11 |
8 |
15 |
16 |
8 |
12 |
10 |
8 |
11 |
9 |
12 |
21 |
21 |
16 |
11 |
12 |
12 |
16 |
8 |
13 |
23 |
21 |
11 |
13 |
12 |
15 |
11 |
12 |
12 |
11 |
Pvt6, Pvt5, Bert
S.4, Jonathan
Samuel3, Jacob2,
Peter1
— of Perry Co., PA |
| These two individuals have a rare haplotype. They have no full
or near matches at 25 or 37 markers (except with each other) making this
haplotype, at least for now, unique and easily distinguishable. We
do not know how these two subjects connect, but I suspect they are
both related to Andreas
STRAUB I, the 1742 immigrant to Lancaster Co., PA. We need a
known patrilineal descendant of Andreas to be tested! |
| Standard testing does not reveal the order of Markers DYS 385a and
385b. By convention, they are reported lo-hi. A Kittler test
can reveal the true order of these alleles; and, in the case of I2b*, Kittler
testing has revealed that their order is actually hi-lo. Your project
admin recommends at least one of you get a Kittler test to determine your
ordering of these alleles. Even though the result is almost certain
to be hi-lo, it's "good science" to be certain. |
| Based on #26031's haplotype, FTDNA tentatively predicted his haplogroup
was "C" (Asian), which prompted a backbone SNP test. The SNP test
result of M216- ruled out Hg C, while P19+ proved Hg I, which shows that,
for rare haplotypes, a backbone SNP test can be essential for determining
the correct haplogroup. |
| Based on Nordtvedt's research, our subjects show an overall resemblance
to the modal haplotype of his I2b*-A variety, yet their haplotype fails
at a key (i.e., extremely slow mutating) marker, namely DYS455 (green
table cells). |
Results of Deep SNP testing for #58687 are:
| I — yes |
I1 — no |
I2a — no |
I1b2a — no |
| P19+ P38+ M170+ M258+ |
P30- M253- M307- M21- M72- M227- |
P37.2- M26- M161- |
M223- |
The positive tests for P19, P38, M170, and M258 prove that he is Hg I,
while the negative results for P30, M253, M307, M21, M72, and M227 rule
out I1 and all of its subclades (see
I1 table), meaning he is proven to be I2. The negative
results for P37.2, M26, and M161 rule out I2a and its subclades (see
I2 table above). The negative result for M223 rules out any subclade
of I2b. So, as predicted by Nordvedt based on the STR haplotype,
our subject is root (ancestral) I2b*. |
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