A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218892



Internal ID20785932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26389378..26389742hg38UCSC Ensembl
chr13:26963515..26963879hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592439
Supporting Variants
Samples
Known GenesCDK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218892
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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