A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691526



Internal ID18643121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:130910285..131682798hg38UCSC Ensembl
Innerchr8:131922531..132695045hg19UCSC Ensembl
Innerchr8:131991713..132764227hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38772514
hg19772515
hg18772515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026579
Supporting Variants
Samples
Known GenesADCY8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691526
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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