A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024399



Internal ID21933742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23108374..23108452hg38UCSC Ensembl
chr14:23577583..23577661hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024399
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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