A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520987



Internal ID15448280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69858186..69858567hg38UCSC Ensembl
Innerchr8:70770421..70770802hg19UCSC Ensembl
Innerchr8:70932975..70933356hg18UCSC Ensembl
Innerchr8:70932975..70933356hg17UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38382
hg19382
hg18382
hg17382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697723
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520987
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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