A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116990



Internal ID21300256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:159276611..159296982hg38UCSC Ensembl
Innerchr5:158703619..158723990hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3820372
hg1920372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097397
Samplessample105
Known GenesUBLCP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116990
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