A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520659



Internal ID15101266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57140959..57808397hg38UCSC Ensembl
Innerchr7:57208666..57868103hg19UCSC Ensembl
Innerchr7:57212608..57872045hg18UCSC Ensembl
Innerchr7:57019323..57678760hg17UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38667439
hg19659438
hg18659438
hg17659438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv674395, nssv683032, nssv704858, nssv673625, nssv679133, nssv704857
Samples
Known GenesGUSBP10, MIR3147, ZNF716
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520659
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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