A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422293



Internal ID201339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52466060..52466111hg38UCSC Ensembl
chr15:52758257..52758308hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702762
Samples
Known GenesMYO5A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422293
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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