A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115121



Internal ID21298387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:133239456..133240715hg38UCSC Ensembl
Innerchr6:133560594..133561853hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086391
Samplessample136
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115121
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