A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594346



Internal ID21786389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89545857..89685808hg38UCSC Ensembl
chr11:89279025..89418976hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38139952
hg19139952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030382
Supporting Variants
Samples
Known GenesFOLH1B, NOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594346
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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