A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686873



Internal ID15076839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176038632..176050237hg38UCSC Ensembl
Innerchr2:176903360..176914965hg19UCSC Ensembl
Innerchr2:176611606..176623211hg18UCSC Ensembl
Innerchr2:176728867..176740472hg17UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3811606
hg1911606
hg1811606
hg1711606
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520227
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686873
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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