A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5901n223



Internal ID22808869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114920001..114935000hg38UCSC Ensembl
chr5:114255698..114270697hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3815000
hg1915000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6398319, nsv6404583
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5901n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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