A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181780



Internal ID20748820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99654207..99672504hg38UCSC Ensembl
chr13:100306461..100324758hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3818298
hg1918298
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491023
Supporting Variants
Samples
Known GenesCLYBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181780
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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