A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520966



Internal ID15448259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75248133..75286004hg38UCSC Ensembl
Innerchr8:76160368..76198239hg19UCSC Ensembl
Innerchr8:76322923..76360794hg18UCSC Ensembl
Innerchr8:76322923..76360794hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3837872
hg1937872
hg1837872
hg1737872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697712
Samples
Known GenesCASC9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520966
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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