A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526314



Internal ID15453607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6809193..6866428hg38UCSC Ensembl
Innerchr4:6810920..6868155hg19UCSC Ensembl
Innerchr4:6861821..6919056hg18UCSC Ensembl
Innerchr4:6928992..6986227hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3857236
hg1957236
hg1857236
hg1757236
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702598
Samples
Known GenesKIAA0232
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526314
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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