A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114344



Internal ID21297610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:180431008..180434296hg38UCSC Ensembl
Innerchr3:180148796..180152084hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg383289
hg193289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108297
Samplessample231
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114344
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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