A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088554



Internal ID21997787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113506285..113506285hg38UCSC Ensembl
chr13:114160600..114160600hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605480
Samples
Known GenesTMCO3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088554
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer