A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279088



Internal ID20488306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68892146..68892146hg38UCSC Ensembl
chr11:68659614..68659614hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762149
Supporting Variants
Samples
Known GenesMRPL21
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279088
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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