A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1022n223



Internal ID22803990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33261431..33470373hg38UCSC Ensembl
chr11:33282977..33491919hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38208943
hg19208943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6455855, nsv6475099
Samples
Known GenesHIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1022n223
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