A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235219



Internal ID20802259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108166089..108166434hg38UCSC Ensembl
chr11:108036816..108037161hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590172
Supporting Variants
Samples
Known GenesNPAT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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