A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222806



Internal ID20789846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102404853..102406615hg38UCSC Ensembl
chr11:102275584..102277346hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381763
hg191763
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593446
Supporting Variants
Samples
Known GenesTMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222806
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