A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1942n223



Internal ID22804910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83501701..83772145hg38UCSC Ensembl
chr13:84075836..84346280hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38270445
hg19270445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6489261, nsv6493527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1942n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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