A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051727



Internal ID102325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133542179..133546973hg38UCSC Ensembl
chr11:133412074..133416868hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384795
hg194795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051727
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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