A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114543



Internal ID21297809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18316026..18651953hg38UCSC Ensembl
Innerchr4:18317649..18653576hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38335928
hg19335928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090539
Samplessample160
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114543
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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