SAMN00249929
EXTERNALSample
- Accession
SAMN00249929- Alias
- HG02155
- Sex
- Female
- Center
- NYGC
- Description
- Human 1000 genomes individual HG02155
- Source publications
Y-DNA pathway
No haplogroup call for this sample.
mtDNA pathway
chrM:5078T>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
-
MchrM:14206T>C, chrM:14466G>A, chrM:16482T>C, chrM:9823C>T
-
DchrM:15785T>C, chrM:4306C>T, chrM:4601C>A
-
D4chrM:14091C>T, chrM:2434G>A, chrM:7837C>T
-
D4gchrM:12527A>G
-
D4g2chrM:16290C>T, chrM:4654G>A
-
D4g2a1chrM:10482C>T, chrM:15697G>A, chrM:3817C>T
-
chrM:5078T>CchrM:11795G>A, chrM:15592C>T, chrM:5078T>C
Origin
Sequencing & coverage
No sequencing data available.
Sequence data & files
Instrument: Illumina NovaSeq 6000 ·
Layout: PAIRED ·
Reads: 698457494 ·
Read length: 150 ·
Date: 2020-05-14
| File | Format | Size | Reference | Aligner | md5 | |
|---|---|---|---|---|---|---|
| HG02155.final.cram | CRAM | — | GRCh38 | bwa mem | 300fe1cd78a0d2d995603fffda681e5a | Download |
Ancestry
No ancestry breakdown available.
Predicted phenotype and genetic-distance metrics are not yet available.