A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv88n206



Internal ID22755392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97744814..97840259hg38UCSC Ensembl
chr11:97615814..97711259hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3895446
hg1995446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5494343, nsv5510943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv88n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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