A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693162



Internal ID15429814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27454979..27558719hg38UCSC Ensembl
Innerchr14:27924185..28027925hg19UCSC Ensembl
Innerchr14:26994025..27097765hg18UCSC Ensembl
Innerchr14:26994025..27097765hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38103741
hg19103741
hg18103741
hg17103741
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520836
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693162
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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