SAMN00780008
EXTERNALSample
- Accession
SAMN00780008- Alias
- HG02684
- Sex
- Male
- Center
- NYGC
- Description
- Human 1000 genomes individual HG02684
- Source publications
Y-DNA pathway
No haplogroup call for this sample.
mtDNA pathway
chrM:3012C>T
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
-
MchrM:14206T>C, chrM:14466G>A, chrM:16482T>C, chrM:9823C>T
-
M3chrM:15549T>C, chrM:16475T>C
-
M3achrM:4003G>A
-
M3a2chrM:10150C>T, chrM:5206G>A
-
chrM:16142C>TchrM:16142C>T
-
chrM:7390C>TchrM:14881T>C, chrM:7390C>T, chrM:8478G>A
-
chrM:3012C>TchrM:10599G>A, chrM:13818T>C, chrM:15592C>T, chrM:3012C>T, chrM:6692G>A
Origin
Sequencing & coverage
No sequencing data available.
Sequence data & files
Instrument: Illumina NovaSeq 6000 ·
Layout: PAIRED ·
Reads: 741331276 ·
Read length: 150 ·
Date: 2020-05-14
| File | Format | Size | Reference | Aligner | md5 | |
|---|---|---|---|---|---|---|
| HG02684.final.cram | CRAM | — | GRCh38 | bwa mem | 81079395bf6ec5690c21b36b296192a7 | Download |
Ancestry
No ancestry breakdown available.
Predicted phenotype and genetic-distance metrics are not yet available.