A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1820n223



Internal ID22804788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46458901..46468100hg38UCSC Ensembl
chr13:47033036..47042235hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6490390, nsv6475708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1820n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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