A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7742n223



Internal ID22810710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41479201..41487900hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6448370, nsv6455550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7742n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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