A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118141



Internal ID21301407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18937923..18957176hg38UCSC Ensembl
Innerchr3:18979415..18998668hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3819254
hg1919254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108354
Samplessample242
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118141
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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