A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111636



Internal ID21294902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113206439..113210896hg38UCSC Ensembl
Innerchr13:113860753..113865210hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384458
hg194458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094578
Samplessample138
Known GenesCUL4A, PCID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111636
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