A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702373



Internal ID15439025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78096373..78134257hg38UCSC Ensembl
Innerchr8:79008608..79046492hg19UCSC Ensembl
Innerchr8:79171163..79209047hg18UCSC Ensembl
Innerchr8:79171163..79209047hg17UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3837885
hg1937885
hg1837885
hg1737885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526123
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702373
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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