A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253582



Internal ID20820622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1673607..1919957hg38UCSC Ensembl
chr20:1654253..1900603hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38246351
hg19246351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599610
Supporting Variants
Samples
Known GenesLOC100289473, SIRPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253582
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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