A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688420



Internal ID112086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94717990..94726765hg38UCSC Ensembl
chr11:94451156..94459931hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388776
hg198776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688420
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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