A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623585



Internal ID21815632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46380683..46382556hg38UCSC Ensembl
chr16:46385802..46416468hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg381874
hg1930667
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102430
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623585
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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