A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115546



Internal ID21298812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:31388119..31394394hg38UCSC Ensembl
Innerchr4:31389741..31396016hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg386276
hg196276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090564
Samplessample163
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115546
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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