A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3892731

Internal ID

19183551

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr15:95566250..95583185	hg38	UCSC Ensembl
Outer	chr15:95565624..95588381	hg38	UCSC Ensembl
Inner	chr15:96109479..96126414	hg19	UCSC Ensembl
Outer	chr15:96108853..96131610	hg19	UCSC Ensembl
Inner	chr15:93910483..93927418	hg18	UCSC Ensembl
Outer	chr15:93909857..93932614	hg18	UCSC Ensembl

Cytoband

15q26.2

Allele length

Assembly	Allele length
hg38	22758
hg19	22758
hg18	22758

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

essv25799680, essv25785795, essv25798554, essv25800473, essv25779187, essv25782764, essv25787250, essv25797034, essv25800650, essv25782204

Samples

Known Genes

Method

SNP array

Analysis

Platform

Illumina HumanHap 610
Illumina Human OmniExpress

Comments

Reference

Suktitipat_et_al_2014

Pubmed ID

Accession Number(s)

Frequency

Sample Size	3017
Observed Gain	0
Observed Loss	10
Observed Complex	0
Frequency	n/a