A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656572



Internal ID15393224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41011504..41034852hg38UCSC Ensembl
Innerchr2:41238644..41261992hg19UCSC Ensembl
Innerchr2:41092148..41115496hg18UCSC Ensembl
Innerchr2:41150295..41173643hg17UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3823349
hg1923349
hg1823349
hg1723349
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515841
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656572
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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