Variant Details

Variant: esv3588590

Internal ID

6628882

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:203095127..203096061	hg38	UCSC Ensembl
Inner	chr1:203095127..203096061	hg38	UCSC Ensembl
Outer	chr1:203094891..203096354	hg38	UCSC Ensembl
	chr1:203064255..203065189	hg19	UCSC Ensembl
Inner	chr1:203064255..203065189	hg19	UCSC Ensembl
Outer	chr1:203064019..203065482	hg19	UCSC Ensembl

Cytoband

1q32.1

Allele length

Assembly	Allele length
hg38	935
hg19	935

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv10265187, essv10265222, essv10265189, essv10265186, essv10265208, essv10265180, essv10265201, essv10265184, essv10265218, essv10265194, essv10265205, essv10265216, essv10265212, essv10265202, essv10265199, essv10265179, essv10265224, essv10265209, essv10265185, essv10265195, essv10265210, essv10265221, essv10265204, essv10265200, essv10265178, essv10265214, essv10265197, essv10265188, essv10265213, essv10265211, essv10265193, essv10265215, essv10265183, essv10265203, essv10265182, essv10265190, essv10265223, essv10265198, essv10265217, essv10265220, essv10265192, essv10265206, essv10265207, essv10265219, essv10265181, essv10265191, essv10265196

Samples

NA19794, NA10851, HG04202, HG04018, HG02734, HG03836, HG01140, HG00641, NA19792, HG01702, NA12283, HG03629, HG00281, NA19651, NA20518, NA20819, HG01527, NA20342, HG04075, HG03884, HG03844, HG02789, HG03730, NA20866, HG02787, HG00110, HG02657, HG03974, HG03740, HG03634, HG02219, NA20542, NA20872, NA20851, HG04219, HG04239, HG03702, HG03488, NA20902, HG03600, HG02654, NA12830, HG03916, HG03894, HG03882, NA20585, HG03985

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3588590

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	47
Observed Complex	0
Frequency	n/a