A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116944



Internal ID21300210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48931537..48936337hg38UCSC Ensembl
Innerchr19:49434794..49439594hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg384801
hg194801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101527
Samplessample370
Known GenesDHDH
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116944
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