A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485059



Internal ID262456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89493603..89496053hg38UCSC Ensembl
chr9:92108518..92110968hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382451
hg192451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485059
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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