A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5904n223



Internal ID22808872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115691188..115820425hg38UCSC Ensembl
chr5:115026885..115156122hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38129238
hg19129238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6409848, nsv6398229
Samples
Known GenesCDO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5904n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer