A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519060



Internal ID15446353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101434859..101435343hg38UCSC Ensembl
Innerchr8:102447087..102447571hg19UCSC Ensembl
Innerchr8:102516263..102516747hg18UCSC Ensembl
Innerchr8:102516263..102516747hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38485
hg19485
hg18485
hg17485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696531
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519060
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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