A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527313



Internal ID15454606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:201834478..201867305hg38UCSC Ensembl
Innerchr2:202699201..202732028hg19UCSC Ensembl
Innerchr2:202407446..202440273hg18UCSC Ensembl
Innerchr2:202524707..202557534hg17UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3832828
hg1932828
hg1832828
hg1732828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703737
Samples
Known GenesCDK15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527313
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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