A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616424



Internal ID21808471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130193864..130193864hg38UCSC Ensembl
chr11:130063759..130063759hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094582
Supporting Variants
Samples
Known GenesST14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616424
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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