A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291463



Internal ID20500681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8053846..8053929hg38UCSC Ensembl
chr11:8075393..8075476hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749402
Supporting Variants
Samples
Known GenesTUB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291463
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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