A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709110



Internal ID132776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66734973..66735638hg38UCSC Ensembl
chr16:66768876..66769541hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556229
Supporting Variants
Samples
Known GenesDYNC1LI2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709110
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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