A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704259



Internal ID15440911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:85722273..85735428hg38UCSC Ensembl
Innerchr2:85949396..85962551hg19UCSC Ensembl
Innerchr2:85802907..85816062hg18UCSC Ensembl
Innerchr2:85861054..85874209hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3813156
hg1913156
hg1813156
hg1713156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527770
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704259
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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