A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051301



Internal ID102061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101143108..101143159hg38UCSC Ensembl
chr11:101013839..101013890hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410572
Supporting Variants
Samples
Known GenesLOC101054525
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051301
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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