A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050176



Internal ID101354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110954101..110954152hg38UCSC Ensembl
chr11:110824825..110824876hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050176
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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