A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628291



Internal ID21820338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89934185..89934185hg38UCSC Ensembl
chr16:90000593..90000593hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097567
Supporting Variants
Samples
Known GenesTUBB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628291
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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