A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694292



Internal ID15430944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:31489555..31514165hg38UCSC Ensembl
Innerchr14:31958761..31983371hg19UCSC Ensembl
Innerchr14:31028512..31053122hg18UCSC Ensembl
Innerchr14:31028512..31053122hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3824611
hg1924611
hg1824611
hg1724611
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518956
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694292
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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