A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590888



Internal ID21539458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116797649..116802971hg38UCSC Ensembl
chr11:116668365..116673687hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385323
hg195323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072832
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590888
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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