A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689707



Internal ID18987988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:90728324..90769013hg38UCSC Ensembl
Innerchr8:91740552..91781241hg19UCSC Ensembl
Innerchr8:91809728..91850417hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3840690
hg1940690
hg1840690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024671
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)nssv3689707
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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