A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045474



Internal ID98076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58908821..58913637hg38UCSC Ensembl
chr11:58676294..58681110hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg384817
hg194817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045474
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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