A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5309n223



Internal ID22808277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68810401..68842000hg38UCSC Ensembl
chr4:69676119..69707718hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3831600
hg1931600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6384023, nsv6378063
Samples
Known GenesUGT2B10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5309n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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