A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116886



Internal ID21300152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37367997..37378237hg38UCSC Ensembl
Innerchr22:37764037..37774277hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3810241
hg1910241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102790
Samplessample116
Known GenesELFN2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116886
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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