A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260505



Internal ID20827545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170268437..170269132hg38UCSC Ensembl
chr3:169986225..169986920hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562081
Supporting Variants
Samples
Known GenesPRKCI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260505
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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