A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234843



Internal ID20801883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79817185..79845799hg38UCSC Ensembl
chr13:80391320..80419934hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3828615
hg1928615
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234843
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00101


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