A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116242



Internal ID21299508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17277454..17516589hg38UCSC Ensembl
Innerchr5:17277563..17516698hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38239136
hg19239136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14109349
Samplessample316
Known GenesLOC401177
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116242
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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