A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116232



Internal ID21299498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:45134888..45139222hg38UCSC Ensembl
Innerchr3:45176380..45180714hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384335
hg194335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105268
Samplessample93
Known GenesCDCP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116232
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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