A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521467



Internal ID15448760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:114805798..114956799hg38UCSC Ensembl
Innerchr3:114524645..114675646hg19UCSC Ensembl
Innerchr3:116007335..116158336hg18UCSC Ensembl
Innerchr3:116007335..116158336hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38151002
hg19151002
hg18151002
hg17151002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698078
Samples
Known GenesZBTB20
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521467
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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