A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499841



Internal ID276796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76373189..76373518hg38UCSC Ensembl
chr11:76084233..76084562hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048533
Samples
Known GenesPRKRIR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499841
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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