A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229135



Internal ID20796175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81099892..81107706hg38UCSC Ensembl
chr13:81674027..81681841hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg387815
hg197815
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595135
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229135
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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