A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113867



Internal ID21297133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36590528..36595494hg38UCSC Ensembl
Innerchr3:36632020..36636986hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg384967
hg194967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv759n145
Supporting Variantsnssv14107890
Samplessample295
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113867
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