A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1924n223



Internal ID22804892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80452189..80469100hg38UCSC Ensembl
chr13:81026324..81043235hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3816912
hg1916912
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6486232, nsv6479241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1924n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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