A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699809



Internal ID15436461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41587034..41622655hg38UCSC Ensembl
Innerchr2:41814174..41849795hg19UCSC Ensembl
Innerchr2:41667678..41703299hg18UCSC Ensembl
Innerchr2:41725825..41761446hg17UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3835622
hg1935622
hg1835622
hg1735622
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523959
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699809
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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