A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766022



Internal ID20541882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68866107..68866107hg38UCSC Ensembl
chr14:69332824..69332824hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382103
hg192103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766022
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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