A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689603



Internal ID18987884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83580982..83632830hg38UCSC Ensembl
Innerchr8:84493217..84545065hg19UCSC Ensembl
Innerchr8:84655772..84707620hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3851849
hg1951849
hg1851849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020324
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)nssv3689603
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer