A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525692



Internal ID15452985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:130854093..130876016hg38UCSC Ensembl
Innerchr8:131866339..131888262hg19UCSC Ensembl
Innerchr8:131935521..131957444hg18UCSC Ensembl
Innerchr8:131935521..131957444hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3821924
hg1921924
hg1821924
hg1721924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701851
Samples
Known GenesADCY8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525692
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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