A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220465



Internal ID20787505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49707997..49709413hg38UCSC Ensembl
chr13:50282133..50283549hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg381417
hg191417
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584670
Supporting Variants
Samples
Known GenesKPNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220465
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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