A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491023



Internal ID21148576
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 StatusM
Merged Variants
Supporting Variantsnssv18181780
Samples
Known GenesCLYBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491023
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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