A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489992



Internal ID267257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99298582..99298637hg38UCSC Ensembl
chr9:102060864..102060919hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025494
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489992
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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