A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100407



Internal ID21272012
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 StatusS
Merged Variantsnsv3115262
Supporting Variants
Samplessample171
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100407
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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