A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17730287



Internal ID153953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1901625..1901832hg38UCSC Ensembl
chr20:1882271..1882478hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523489
Supporting Variants
Samples
Known GenesSIRPA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17730287
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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