A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662924



Internal ID15399576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20925130..20931418hg38UCSC Ensembl
Innerchr14:21393289..21399577hg19UCSC Ensembl
Innerchr14:20463129..20469417hg18UCSC Ensembl
Innerchr14:20463129..20469417hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg386289
hg196289
hg186289
hg176289
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517174
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662924
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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