A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704133



Internal ID15440785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28438654..28447252hg38UCSC Ensembl
Innerchr8:28296171..28304769hg19UCSC Ensembl
Innerchr8:28352090..28360688hg18UCSC Ensembl
Innerchr8:28352090..28360688hg17UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg388599
hg198599
hg188599
hg178599
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527661
Supporting Variants
Samples
Known GenesFBXO16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704133
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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