A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501379



Internal ID278278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59477074..59492000hg38UCSC Ensembl
chr11:59244547..59259473hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3814927
hg1914927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045511
Samples
Known GenesOR4D10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501379
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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