A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093265



Internal ID22002498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99729986..99729986hg38UCSC Ensembl
chr13:100382240..100382240hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605633
Samples
Known GenesCLYBL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093265
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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