A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052276



Internal ID102699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119630344..119630398hg38UCSC Ensembl
chr11:119501055..119501109hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052276
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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