A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486627



Internal ID263988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19789783..19810245hg38UCSC Ensembl
chr9:19789781..19810243hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3820463
hg1920463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486627
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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