A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691269



Internal ID18642864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:108409654..108465656hg38UCSC Ensembl
Innerchr8:109421883..109477885hg19UCSC Ensembl
Innerchr8:109491059..109547061hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3856003
hg1956003
hg1856003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028422
Supporting Variants
Samples
Known GenesEMC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691269
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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