A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240894



Internal ID20807934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87362667..87363287hg38UCSC Ensembl
chr16:87396273..87396893hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595177
Supporting Variants
Samples
Known GenesFBXO31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240894
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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