A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489486



Internal ID266764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87815538..87815603hg38UCSC Ensembl
chr9:90430453..90430518hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489486
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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