A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523491



Internal ID15104098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5500146..5678104hg38UCSC Ensembl
Innerchr10:5542109..5720067hg19UCSC Ensembl
Innerchr10:5532109..5760073hg18UCSC Ensembl
Innerchr10:5532109..5760073hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38177959
hg19177959
hg18227965
hg17227965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699258
Samples
Known GenesASB13, CALML3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523491
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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