A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5228n223



Internal ID22808196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35020101..35056500hg38UCSC Ensembl
chr4:35021723..35058122hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3836400
hg1936400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6369010, nsv6359451, nsv6357186, nsv6374952
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5228n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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