A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222658



Internal ID20789698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79331022..79331465hg38UCSC Ensembl
chr13:79905157..79905600hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575923
Supporting Variants
Samples
Known GenesRBM26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222658
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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