A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406879



Internal ID22464749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9213104..9213377hg38UCSC Ensembl
chr20:9193751..9194024hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935907
Supporting Variants
Samples
Known GenesPLCB4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406879
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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