A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525612



Internal ID15452905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78096373..78134460hg38UCSC Ensembl
Innerchr8:79008608..79046695hg19UCSC Ensembl
Innerchr8:79171163..79209250hg18UCSC Ensembl
Innerchr8:79171163..79209250hg17UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3838088
hg1938088
hg1838088
hg1738088
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv461n21
Supporting Variantsnssv701757
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525612
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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