A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv295n21



Internal ID20132016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116676731..116866434hg38UCSC Ensembl
chr3:116395578..116585281hg19UCSC Ensembl
chr3:117878268..118067971hg18UCSC Ensembl
chr3:117878268..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 Variants
Supporting Variantsnsv524961, nsv521250
Samples
Known GenesTUSC7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv295n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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