A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059161



Internal ID107308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88108238..88108289hg38UCSC Ensembl
chr11:87841406..87841457hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5401263
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17059161
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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