A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116409



Internal ID21299675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33372902..33376313hg38UCSC Ensembl
Innerchr19:33863808..33867219hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383412
hg193412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv564n145
Supporting Variantsnssv14100370, nssv14101364
Samplessample306, sample158
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116409
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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