A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532094



Internal ID308025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59240722..59242395hg38UCSC Ensembl
chr15:59532921..59534594hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381674
hg191674
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700949
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532094
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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