A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051402



Internal ID102125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109709591..109746973hg38UCSC Ensembl
chr11:109580317..109617699hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3837383
hg1937383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509418
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051402
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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