A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501562



Internal ID278456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15786000..15795000hg38UCSC Ensembl
chr11:15807546..15816546hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg389001
hg199001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501562
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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