A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522630



Internal ID298894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59368769..59390436hg38UCSC Ensembl
chr15:59660968..59682635hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3821668
hg1921668
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700956
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522630
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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