A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111842



Internal ID21295108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:86284651..86289622hg38UCSC Ensembl
Innerchr3:86333801..86338772hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg384972
hg194972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108534
Samplessample354
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111842
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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