A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583841



Internal ID20956912
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 StatusM
Merged Variants
Supporting Variantsnssv18225254
Samples
Known GenesRUFY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583841
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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