Variant Details

Variant: esv2665506

Internal ID

9584925

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr19:13831302..13831408	hg38	UCSC Ensembl
Outer	chr19:13830931..13831778	hg38	UCSC Ensembl
Inner	chr19:13942116..13942222	hg19	UCSC Ensembl
Outer	chr19:13941745..13942592	hg19	UCSC Ensembl

Cytoband

19p13.13

Allele length

Assembly	Allele length
hg38	848
hg19	848

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6143623, essv6305111, essv6554284, essv5518865, essv5552302, essv5643663, essv5992829, essv6058329, essv5989351, essv5399181, essv6447530, essv6423668, essv5890167, essv6016983, essv6123436, essv6462166, essv6457803, essv6289303, essv6201357, essv6387830, essv6518991, essv5685392, essv5831397, essv6529660, essv5671284, essv5964959, essv5433041, essv6165651, essv6449298, essv5451423, essv5474591, essv5908180, essv6234267, essv5763527, essv5942540, essv6167180, essv6385936, essv6315454, essv6383223, essv5430592, essv5590656, essv6578905, essv6500188, essv6520927, essv5408113, essv6236340, essv5965001, essv5783549, essv5471930, essv5851907

Samples

HG00734, HG01072, HG01052, HG01075, HG01055, HG01173, HG01083, HG00731, HG01098, HG01079, HG01197, HG01051, HG01082, HG01174, HG00553, HG01182, HG01167, HG01188, HG01204, HG01101, HG01168, HG00737, HG01171, HG00554, HG01107, HG01048, HG01061, HG01183, HG01047, HG01187, HG01097, HG01191, HG00640, HG01066, HG00732, HG01073, HG01170, HG01069, HG01176, HG01080, HG00740, HG01070, HG01060, HG01190, HG01095, HG01108, HG00641, HG01102, HG01067, HG01198

Known Genes

ZSWIM4

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2665506

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	50
Observed Complex	0
Frequency	n/a