A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657241



Internal ID15393893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11065233..11065295hg38UCSC Ensembl
Innerchr2:11205359..11205421hg19UCSC Ensembl
Innerchr2:11122810..11122872hg18UCSC Ensembl
Innerchr2:11155957..11156019hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3863
hg1963
hg1863
hg1763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516163
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657241
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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