A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254091



Internal ID20821131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63631797..63638995hg38UCSC Ensembl
chr20:62263150..62270348hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg387199
hg197199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598015
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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