A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103166



Internal ID21283668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:18021887..18025274hg38UCSC Ensembl
Innerchr22:18504653..18508040hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg383388
hg193388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115200
Supporting Variants
Samplessample348
Known GenesMICAL3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103166
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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