A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691478



Internal ID18989759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121304808..121338697hg38UCSC Ensembl
Innerchr8:122317048..122350937hg19UCSC Ensembl
Innerchr8:122386229..122420118hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3833890
hg1933890
hg1833890
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028470
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)nssv3691478
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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