A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111239



Internal ID21294505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:63080911..63087475hg38UCSC Ensembl
Innerchr5:62376738..62383302hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg386565
hg196565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082561
Samplessample366
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111239
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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