A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497360



Internal ID274399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66677093..66677762hg38UCSC Ensembl
chr11:66444564..66445233hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046216
Samples
Known GenesRBM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497360
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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