A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491833



Internal ID21149386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112473424..112788219hg38UCSC Ensembl
chr13:113127738..113442533hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38314796
hg19314796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193175
Samples
Known GenesATP11A, C13orf35, TUBGCP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491833
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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