A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225054



Internal ID20792094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38631545..38633890hg38UCSC Ensembl
chr11:38653095..38655440hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382346
hg192346
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590698
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225054
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00081


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