A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294852



Internal ID20504070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89933968..89933968hg38UCSC Ensembl
chr16:90000376..90000376hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752874
Supporting Variants
Samples
Known GenesTUBB3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294852
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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