A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113116



Internal ID21296382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120051659..120864642hg38UCSC Ensembl
Innerchr5:119387354..120200337hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38812984
hg19812984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096681
Samplessample6
Known GenesPRR16
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113116
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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