A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760624



Internal ID20536484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55456346..55456346hg38UCSC Ensembl
chr14:55923064..55923064hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760624
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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