A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225254



Internal ID20792294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68390876..68391451hg38UCSC Ensembl
chr10:70150633..70151208hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583841
Supporting Variants
Samples
Known GenesRUFY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225254
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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