A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116573



Internal ID21299839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43186469..43211709hg38UCSC Ensembl
Innerchr4:43188486..43213726hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3825241
hg1925241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14107610
Samplessample87
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116573
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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