A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115262



Internal ID21298528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33372902..33376385hg38UCSC Ensembl
Innerchr19:33863808..33867291hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383484
hg193484
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv564n145
Supporting Variantsnssv14100407, nssv14101533, nssv14100382
Samplessample171, sample372, sample162
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115262
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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