A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730239



Internal ID153905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1161022..1161130hg38UCSC Ensembl
chr20:1141666..1141774hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515758
Supporting Variants
Samples
Known GenesPSMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730239
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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