A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089342



Internal ID21998575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113506388..113506388hg38UCSC Ensembl
chr13:114160703..114160703hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608028
Samples
Known GenesTMCO3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089342
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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