A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242664



Internal ID20809704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22930500..22931265hg38UCSC Ensembl
chr16:22941821..22942586hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242664
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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