A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117892



Internal ID21301158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190025014..190042137hg38UCSC Ensembl
Innerchr3:189742803..189759926hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3817124
hg1917124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108147
Samplessample205
Known GenesLEPREL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117892
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