A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526092



Internal ID15453385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9086797..9124886hg38UCSC Ensembl
Innerchr8:8944307..8982396hg19UCSC Ensembl
Innerchr8:8981717..9019806hg18UCSC Ensembl
Innerchr8:8981717..9019806hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3838090
hg1938090
hg1838090
hg1738090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv446n21
Supporting Variantsnssv702339
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526092
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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