A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635980



Internal ID21828027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89934006..89934006hg38UCSC Ensembl
chr16:90000414..90000414hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087526
Supporting Variants
Samples
Known GenesTUBB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635980
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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