A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097567



Internal ID22006800
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 StatusM
Merged Variants
Supporting Variantsnssv17628291
Samples
Known GenesTUBB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097567
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer