A curated catalogue of human genomic structural variation

Variant Details

Variant: esv3892013

Internal ID

19186409

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr11:55853223..55922895	hg38	UCSC Ensembl
Outer	chr11:55828837..55928509	hg38	UCSC Ensembl
Inner	chr11:55620699..55690371	hg19	UCSC Ensembl
Outer	chr11:55596313..55695985	hg19	UCSC Ensembl
Inner	chr11:55377275..55446947	hg18	UCSC Ensembl
Outer	chr11:55352889..55452561	hg18	UCSC Ensembl

Cytoband

11q11

Allele length

Assembly	Allele length
hg38	99673
hg19	99673
hg18	99673

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

essv25789654, essv25792066, essv25788455, essv25789360, essv25790977, essv25788976, essv25789215, essv25790624

Samples

Known Genes

OR5D16, OR5W2, TRIM51

Method

SNP array

Analysis

Platform

Illumina HumanHap 610

Comments

Reference

Suktitipat_et_al_2014

Pubmed ID

Accession Number(s)

Frequency

Sample Size	3017
Observed Gain	8
Observed Loss	0
Observed Complex	0
Frequency	n/a