A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114432



Internal ID21297698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32630839..32643593hg38UCSC Ensembl
Innerchr3:32672331..32685085hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3812755
hg1912755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108714
Samplessample386
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114432
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