A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045177



Internal ID97869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65080887..65081052hg38UCSC Ensembl
chr11:64848359..64848524hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503438
Supporting Variants
Samples
Known GenesCDCA5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045177
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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