A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257106



Internal ID20824147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197468732..197469374hg38UCSC Ensembl
chr2:198333456..198334098hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553712
Supporting Variants
Samples
Known GenesCOQ10B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257106
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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