A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657887



Internal ID15394539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14565266..14573860hg38UCSC Ensembl
Innerchr2:14705390..14713984hg19UCSC Ensembl
Innerchr2:14622841..14631435hg18UCSC Ensembl
Innerchr2:14655988..14664582hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg388595
hg198595
hg188595
hg178595
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516976
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657887
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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