A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523259



Internal ID15103866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94774827..94933970hg38UCSC Ensembl
Innerchr10:96534584..96693727hg19UCSC Ensembl
Innerchr10:96524574..96683717hg18UCSC Ensembl
Innerchr10:96524574..96683717hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38159144
hg19159144
hg18159144
hg17159144
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698991
Samples
Known GenesCYP2C19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523259
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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