A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766366



Internal ID20542226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70531428..70531428hg38UCSC Ensembl
chr15:70823767..70823767hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766366
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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