A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5364n223



Internal ID22808332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91572455..92413857hg38UCSC Ensembl
chr4:92493606..93335008hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38841403
hg19841403
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6390479, nsv6376045
Samples
Known GenesCCSER1, GRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5364n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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