A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091489



Internal ID22000722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73850440..73850440hg38UCSC Ensembl
chr11:73561485..73561485hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381141
hg191141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585951
Samples
Known GenesMRPL48
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091489
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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