A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523489



Internal ID299720
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 StatusM
Merged Variants
Supporting Variantsnssv17730287
Samples
Known GenesSIRPA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523489
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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