A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280111



Internal ID20489329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123371084..123371084hg38UCSC Ensembl
chr11:123241792..123241792hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759768
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280111
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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