A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040119



Internal ID21949462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59282900..59282992hg38UCSC Ensembl
chr15:59575099..59575191hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612029
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040119
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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