A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223640



Internal ID20790680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109006855..109007449hg38UCSC Ensembl
chr11:108877582..108878176hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223640
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