A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498244



Internal ID275241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102543621..102554619hg38UCSC Ensembl
chr11:102414352..102425350hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3810999
hg1910999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498244
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