A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507562



Internal ID284277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133542179..133546973hg38UCSC Ensembl
chr11:133412074..133416868hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384795
hg194795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507562
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer