A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702271



Internal ID15438923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:86878321..86881088hg38UCSC Ensembl
Innerchr2:87105444..87108211hg19UCSC Ensembl
Innerchr2:86958955..86961722hg18UCSC Ensembl
Innerchr2:87017102..87019869hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg382768
hg192768
hg182768
hg172768
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516466
Supporting Variants
Samples
Known GenesANAPC1P1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702271
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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