A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236818



Internal ID20803858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95471743..95472659hg38UCSC Ensembl
chr13:96123997..96124913hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592103
Supporting Variants
Samples
Known GenesCLDN10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236818
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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