A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519737



Internal ID15447030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144910481..144946051hg38UCSC Ensembl
Innerchr8:146135866..146171437hg19UCSC Ensembl
Innerchr8:146106670..146142241hg18UCSC Ensembl
Innerchr8:146106670..146142241hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3835571
hg1935572
hg1835572
hg1735572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697021
Samples
Known GenesZNF16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519737
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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