A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279975



Internal ID20489193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118947978..118947978hg38UCSC Ensembl
chr11:118818688..118818688hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759056
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279975
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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