A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524961



Internal ID15105568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116676731..116866434hg38UCSC Ensembl
Innerchr3:116395578..116585281hg19UCSC Ensembl
Innerchr3:117878268..118067971hg18UCSC Ensembl
Innerchr3:117878268..118067971hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38189704
hg19189704
hg18189704
hg17189704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv295n21
Supporting Variantsnssv700982
Samples
Known GenesTUSC7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524961
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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