A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084516



Internal ID21993749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109149980..109149980hg38UCSC Ensembl
chr9:111912260..111912260hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587340
Samples
Known GenesFRRS1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084516
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