A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114382



Internal ID21297648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23290596..23297426hg38UCSC Ensembl
Innerchr9:23290594..23297424hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg386831
hg196831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1225n145
Supporting Variantsnssv14088897, nssv14088055
Samplessample312, sample424
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114382
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer