A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098298



Internal ID22007531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22818688..22818688hg38UCSC Ensembl
chr16:22830009..22830009hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602158
Samples
Known GenesHS3ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098298
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