A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103641



Internal ID21272768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35568327..35570488hg38UCSC Ensembl
Innerchr22:35964374..35966535hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382162
hg192162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110284
Supporting Variants
Samplessample182
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103641
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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