A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753961



Internal ID20529821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59282860..59282860hg38UCSC Ensembl
chr15:59575059..59575059hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294001
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753961
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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