A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526123



Internal ID15453416
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 StatusM
Merged Variantsdgv461n21
Supporting Variantsnssv702373
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526123
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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