A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220895



Internal ID20787935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108108166..108108642hg38UCSC Ensembl
chr11:107978893..107979369hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595537
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220895
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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