A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697940



Internal ID15434592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20734056..20735000hg38UCSC Ensembl
Innerchr14:21202215..21203159hg19UCSC Ensembl
Innerchr14:20272055..20272999hg18UCSC Ensembl
Innerchr14:20272055..20272999hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38945
hg19945
hg18945
hg17945
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521333
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697940
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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