A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697626



Internal ID15434278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19837272..19998665hg38UCSC Ensembl
Innerchr14:20305431..20466824hg19UCSC Ensembl
Innerchr14:19375271..19536664hg18UCSC Ensembl
Innerchr14:19375271..19536664hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38161394
hg19161394
hg18161394
hg17161394
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520814
Supporting Variants
Samples
Known GenesOR4K1, OR4K15, OR4K2, OR4K5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697626
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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