A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691283



Internal ID18989564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110494216..110517356hg38UCSC Ensembl
Innerchr8:111506445..111529585hg19UCSC Ensembl
Innerchr8:111575621..111598761hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3823141
hg1923141
hg1823141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021822
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691283
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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