A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102637



Internal ID21285142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36741703..36750906hg38UCSC Ensembl
Innerchr22:37137748..37146950hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg389204
hg199203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116244
Supporting Variants
Samplessample37
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102637
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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