SAMN00263049
EXTERNALSample
- Accession
SAMN00263049- Alias
- HG02382
- Sex
- Male
- Center
- NYGC
- Description
- Human 1000 genomes individual HG02382
- Source publications
Y-DNA pathway
No haplogroup call for this sample.
mtDNA pathway
chrM:11155T>C
From de-novo tree placement
-
L1'2'3'4'5'6'7chrM:16181G>A
-
L2'3'4'5'6'7chrM:12528G>A, chrM:15734C>T, chrM:16187C>T, chrM:2182A>G, chrM:2309C>T, chrM:6569G>A, chrM:7891T>C
-
L2'3'4'6chrM:10111A>G, chrM:10233C>T, chrM:12929T>C, chrM:14724G>A, chrM:15610T>C, chrM:249A>T, chrM:8078T>C
-
L3'4chrM:13073T>C, chrM:15701T>C, chrM:16174T>C, chrM:3017T>C, chrM:3527G>A, chrM:6679T>C, chrM:6944A>G
-
L3chrM:193A>G, chrM:442A>G
-
NchrM:10296C>T, chrM:14724A>G, chrM:8124G>A, chrM:8963C>T
-
RchrM:15646T>C
-
R9chrM:13351G>C, chrM:3393C>T
-
R9b1chrM:12137T>C, chrM:15732A>G, chrM:15813G>A, chrM:965T>C
-
R9b1a3chrM:2627C>T, chrM:2739G>A, chrM:6238T>C
-
chrM:9524T>CchrM:9524T>C
-
chrM:11155T>CchrM:11155T>C, chrM:14043C>T, chrM:15474A>G
Origin
Sequencing & coverage
No sequencing data available.
Sequence data & files
Instrument: Illumina NovaSeq 6000 ·
Layout: PAIRED ·
Reads: 699916738 ·
Read length: 150 ·
Date: 2020-05-14
| File | Format | Size | Reference | Aligner | md5 | |
|---|---|---|---|---|---|---|
| HG02382.final.cram | CRAM | — | GRCh38 | bwa mem | 4a41abeb9418f07320f3f092960ee01a | Download |
Ancestry
No ancestry breakdown available.
Predicted phenotype and genetic-distance metrics are not yet available.