A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639234



Internal ID21831281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37881285..37882631hg38UCSC Ensembl
chr22:38277292..38278638hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381347
hg191347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051138
Supporting Variants
Samples
Known GenesEIF3L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639234
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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