A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117790



Internal ID21301056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33373050..33376385hg38UCSC Ensembl
Innerchr19:33863956..33867291hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383336
hg193336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv564n145
Supporting Variantsnssv14101373
Samplessample309
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117790
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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