A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521033



Internal ID15448326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:103081131..103098347hg38UCSC Ensembl
Innerchr8:104093359..104110575hg19UCSC Ensembl
Innerchr8:104162535..104179751hg18UCSC Ensembl
Innerchr8:104162535..104179751hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3817217
hg1917217
hg1817217
hg1717217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697745
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521033
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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