A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5899n223



Internal ID22808867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114689901..114698500hg38UCSC Ensembl
chr5:114025598..114034197hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6409775, nsv6408387, nsv6414951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5899n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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