A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1988n223



Internal ID22804956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104382701..104393000hg38UCSC Ensembl
chr13:105035051..105045350hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6487521, nsv6482518, nsv6495028
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1988n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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