A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517881



Internal ID15098488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:70979496..71058210hg38UCSC Ensembl
Innerchr2:71206626..71285340hg19UCSC Ensembl
Innerchr2:71060134..71138848hg18UCSC Ensembl
Innerchr2:71118281..71196995hg17UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3878715
hg1978715
hg1878715
hg1778715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695289
Samples
Known GenesANKRD53, OR7E91P, TEX261
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517881
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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