A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751426



Internal ID20527286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73795960..73795960hg38UCSC Ensembl
chr14:74262663..74262663hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751426
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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