A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234810



Internal ID20801850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125567711..125568842hg38UCSC Ensembl
chr11:125437607..125438738hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234810
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