A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050335



Internal ID101457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116584590..116589928hg38UCSC Ensembl
chr11:116455307..116460645hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385339
hg195339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513028
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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