A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114381



Internal ID21297647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:225122422..225124356hg38UCSC Ensembl
Innerchr2:225987139..225989073hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg381935
hg191935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv669n145
Supporting Variantsnssv14103838
Samplessample118
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114381
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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