A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115248



Internal ID21298514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33374309..33375045hg38UCSC Ensembl
Innerchr19:33865215..33865951hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100492
Samplessample208
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115248
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer