A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4425n223



Internal ID22807393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23685903..23759094hg38UCSC Ensembl
chr20:23666540..23739731hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3873192
hg1973192
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6515791, nsv6525597
Samples
Known GenesCST1, CST4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4425n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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