A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362276



Internal ID22587945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98594342..98653033hg38UCSC Ensembl
chr11:98465072..98523763hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3858692
hg1958692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918887
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362276
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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