A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686276



Internal ID15422928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35593041..35862576hg38UCSC Ensembl
Innerchr2:35818107..36087642hg19UCSC Ensembl
Innerchr2:35671611..35941146hg18UCSC Ensembl
Innerchr2:35729758..35999293hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38269536
hg19269536
hg18269536
hg17269536
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519867
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686276
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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