A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5928n223



Internal ID22808896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122509301..122518900hg38UCSC Ensembl
chr5:121844996..121854595hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6411639, nsv6408902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5928n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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