A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042998



Internal ID96372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16758051..16758151hg38UCSC Ensembl
chr11:16779598..16779698hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503168
Supporting Variants
Samples
Known GenesC11orf58
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042998
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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