A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658988



Internal ID15048954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43169482..43936548hg38UCSC Ensembl
Innerchr8:43024625..43791691hg19UCSC Ensembl
Innerchr8:43143782..43910848hg18UCSC Ensembl
Innerchr8:43143782..43910848hg17UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38767067
hg19767067
hg18767067
hg17767067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519841
Supporting Variants
Samples
Known GenesHGSNAT, POTEA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658988
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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