A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051488



Internal ID102178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121806809..121867660hg38UCSC Ensembl
chr11:121677517..121738368hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3860852
hg1960852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497315
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051488
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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