A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691081



Internal ID15427733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41011504..41018361hg38UCSC Ensembl
Innerchr2:41238644..41245501hg19UCSC Ensembl
Innerchr2:41092148..41099005hg18UCSC Ensembl
Innerchr2:41150295..41157152hg17UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg386858
hg196858
hg186858
hg176858
Variant TypeCNV gain
Copy Number
Allele State
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)nssv691081
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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