A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5076n223



Internal ID22808044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:166062301..166257500hg38UCSC Ensembl
chr3:165780089..165975288hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38195200
hg19195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6360389, nsv6357244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5076n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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