A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052222



Internal ID102669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119038525..119041685hg38UCSC Ensembl
chr11:118909235..118912395hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383161
hg193161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052222
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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