A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051021



Internal ID101889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:91765642..91766116hg38UCSC Ensembl
chr11:91498808..91499282hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051021
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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