A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754566



Internal ID20530426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24696867..24696867hg38UCSC Ensembl
chr14:25166073..25166073hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754566
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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