A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352471



Internal ID22578140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122955185..122955315hg38UCSC Ensembl
chr11:122825893..122826023hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910089
Supporting Variants
Samples
Known GenesC11orf63
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352471
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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