A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024343



Internal ID21933686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59712708..59715620hg38UCSC Ensembl
chr14:60179426..60182338hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg382913
hg192913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602088
Samples
Known GenesRTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024343
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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