A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622552



Internal ID21814599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45721509..45724068hg38UCSC Ensembl
chr19:46224767..46227326hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382560
hg192560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055192
Supporting Variants
Samples
Known GenesFBXO46
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622552
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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