A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111019



Internal ID21294285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112894078..112915950hg38UCSC Ensembl
Innerchr3:112612925..112634797hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3821873
hg1921873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104531, nssv14108522
Samplessample350, sample88
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111019
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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