A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244342



Internal ID20811382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69443093..69443578hg38UCSC Ensembl
chr16:69476996..69477481hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586020
Supporting Variants
Samples
Known GenesCYB5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244342
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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