A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110391



Internal ID21293657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:37322774..37325075hg38UCSC Ensembl
Innerchr2:37549917..37552218hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg382302
hg192302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106296
Samplessample348
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110391
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