A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689683



Internal ID18641278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86249473..86355705hg38UCSC Ensembl
Innerchr8:87261702..87367934hg19UCSC Ensembl
Innerchr8:87330818..87437050hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38106233
hg19106233
hg18106233
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017535
Supporting Variants
Samples
Known GenesWWP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689683
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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