A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527453



Internal ID15454746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:19909300..19960448hg38UCSC Ensembl
Innerchr2:20109061..20160209hg19UCSC Ensembl
Innerchr2:19972542..20023690hg18UCSC Ensembl
Innerchr2:20030689..20081837hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3851149
hg1951149
hg1851149
hg1751149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703894
Samples
Known GenesWDR35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527453
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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