A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891075



Internal ID168226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160408730..160409794hg38UCSC Ensembl
chr1:160378520..160379584hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556352
Supporting Variants
Samples
Known GenesVANGL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891075
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