A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521358



Internal ID15448651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131292261..131339904hg38UCSC Ensembl
Innerchr8:132304508..132352151hg19UCSC Ensembl
Innerchr8:132373690..132421333hg18UCSC Ensembl
Innerchr8:132373690..132421333hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3847644
hg1947644
hg1847644
hg1747644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697968
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521358
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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