A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102927



Internal ID21276268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:32481526..32488408hg38UCSC Ensembl
Innerchr22:32877513..32884395hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg386883
hg196883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112822
Supporting Variants
Samplessample234
Known GenesFBXO7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102927
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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