A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv92n206



Internal ID22755396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109130714..109162892hg38UCSC Ensembl
chr11:109001441..109033619hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3832179
hg1932179
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5513086, nsv5495859
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv92n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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