A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230211



Internal ID20797251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59573753..59574084hg38UCSC Ensembl
chr13:60147887..60148218hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230211
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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