A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111716



Internal ID21294982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:21574637..21600217hg38UCSC Ensembl
Innerchr5:21574746..21600326hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3825581
hg1925581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097267
Samplessample78
Known GenesGUSBP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111716
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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