A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1168n223



Internal ID22804136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50791801..50821400hg38UCSC Ensembl
chr11:50750972..50780519hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3829600
hg1929548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6465858, nsv6473338, nsv6464499, nsv6462050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1168n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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