A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230458



Internal ID20797498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97912025..97912102hg38UCSC Ensembl
chr13:98564279..98564356hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230458
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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