A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3456n223



Internal ID22806424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18298403..18303982hg38UCSC Ensembl
chr19:18409213..18414792hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg385580
hg195580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6533389, nsv6533106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3456n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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