A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4451n223



Internal ID22807419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34528001..34529800hg38UCSC Ensembl
chr20:33115806..33117604hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381800
hg191799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6521631, nsv6532473
Samples
Known GenesDYNLRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4451n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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