A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494570



Internal ID21152123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110042000..110052697hg38UCSC Ensembl
chr13:110694347..110705044hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3810698
hg1910698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494570
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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