A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502548



Internal ID279409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109881295..109881484hg38UCSC Ensembl
chr11:109752021..109752210hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502548
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