A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1821n223



Internal ID22804789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46805501..46811700hg38UCSC Ensembl
chr13:47379636..47385835hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6483867, nsv6488149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1821n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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