A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046747



Internal ID98978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65451624..65451850hg38UCSC Ensembl
chr11:65219095..65219321hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046747
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.034666


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