A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5263n223



Internal ID22808231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51811201..51896000hg38UCSC Ensembl
chr4:52677367..52762166hg19UCSC Ensembl
Cytoband4q11
Allele length
AssemblyAllele length
hg3884800
hg1984800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6386411, nsv6380554
Samples
Known GenesDCUN1D4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5263n223
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