A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114540



Internal ID21297806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36993801..37013699hg38UCSC Ensembl
Innerchr22:37389842..37409740hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3819899
hg1919899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14103061
Samplessample296
Known GenesTEX33, TST
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114540
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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