A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230879



Internal ID20797919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27894920..27895463hg38UCSC Ensembl
chr13:28469057..28469600hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580986
Supporting Variants
Samples
Known GenesPDX1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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