A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117830



Internal ID21301096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33371984..33376385hg38UCSC Ensembl
Innerchr19:33862890..33867291hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384402
hg194402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv563n145
Supporting Variantsnssv14101009
Samplessample11
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117830
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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