A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116747



Internal ID21300013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81813321..82004630hg38UCSC Ensembl
Innerchr5:81109140..81300449hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38191310
hg19191310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097270
Samplessample78
Known GenesATG10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116747
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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