A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1319n223



Internal ID22804287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116149301..116151900hg38UCSC Ensembl
chr11:116020018..116022617hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6463548, nsv6465034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1319n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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