A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695416



Internal ID15432068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:36118862..36341871hg38UCSC Ensembl
Innerchr2:36346005..36569014hg19UCSC Ensembl
Innerchr2:36199509..36422518hg18UCSC Ensembl
Innerchr2:36257656..36480665hg17UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38223010
hg19223010
hg18223010
hg17223010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518004
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695416
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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