A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085519



Internal ID21994752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113508986..113508986hg38UCSC Ensembl
chr13:114163301..114163301hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601760
Samples
Known GenesTMCO3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085519
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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