A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050695



Internal ID101676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107682031..107787122hg38UCSC Ensembl
chr11:107552757..107657848hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38105092
hg19105092
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505974
Supporting Variants
Samples
Known GenesSLN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050695
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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