A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497787



Internal ID274811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24354297..24486350hg38UCSC Ensembl
chr11:24375843..24507896hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38132054
hg19132054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497787
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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