A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4553n223



Internal ID22807521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17346946..17766164hg38UCSC Ensembl
chr21:18719265..19138481hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38419219
hg19419217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6535650, nsv6542916
Samples
Known GenesBTG3, C21orf37, CXADR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4553n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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