A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233588



Internal ID20800628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:23341882..23343484hg38UCSC Ensembl
chr13:23916021..23917623hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381603
hg191603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592329
Supporting Variants
Samples
Known GenesSACS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233588
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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