A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766536



Internal ID20542396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98063631..98063631hg38UCSC Ensembl
chr13:98715885..98715885hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766536
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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