A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691482



Internal ID18989763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121391755..121426457hg38UCSC Ensembl
Innerchr8:122403995..122438697hg19UCSC Ensembl
Innerchr8:122473176..122507878hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3834703
hg1934703
hg1834703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018781
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)nssv3691482
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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