A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513728



Internal ID290244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62325417..62389621hg38UCSC Ensembl
chr11:62092889..62157093hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3864205
hg1964205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046640
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513728
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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