A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294001



Internal ID20503219
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 StatusS
Merged Variantsnsv4753961
Supporting Variants
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294001
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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