A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254350



Internal ID20821390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37216107..37216569hg38UCSC Ensembl
chr20:35844510..35844972hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598186
Supporting Variants
Samples
Known GenesRPN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254350
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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