A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496691



Internal ID273761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92498629..92511101hg38UCSC Ensembl
chr11:92231795..92244267hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3812473
hg1912473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051069
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496691
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