A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114062



Internal ID21297328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4084850..4199999hg38UCSC Ensembl
Innerchr3:4126534..4241683hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38115150
hg19115150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108375
Samplessample244
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114062
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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