A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520442



Internal ID15447735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62016156..62049512hg38UCSC Ensembl
Innerchr8:62928715..62962071hg19UCSC Ensembl
Innerchr8:63091269..63124625hg18UCSC Ensembl
Innerchr8:63091269..63124625hg17UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3833357
hg1933357
hg1833357
hg1733357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702665, nssv671504, nssv678691
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520442
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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