A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515758



Internal ID292235
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 StatusM
Merged Variants
Supporting Variantsnssv17730239
Samples
Known GenesPSMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515758
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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