A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115099



Internal ID21298365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33373338..33377047hg38UCSC Ensembl
Innerchr19:33864244..33867953hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383710
hg193710
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv564n145
Supporting Variantsnssv14101541
Samplessample373
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115099
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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