A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114038



Internal ID21297304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:21750805..21752345hg38UCSC Ensembl
Innerchr21:23123125..23124665hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381541
hg191541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv702n145
Supporting Variantsnssv14102006
Samplessample196
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114038
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