A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652384



Internal ID15389036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41011504..41048432hg38UCSC Ensembl
Innerchr2:41238644..41275572hg19UCSC Ensembl
Innerchr2:41092148..41129076hg18UCSC Ensembl
Innerchr2:41150295..41187223hg17UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3836929
hg1936929
hg1836929
hg1736929
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)nssv652384
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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