A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481034



Internal ID258529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87426760..87439047hg38UCSC Ensembl
chr9:90041675..90053962hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3812288
hg1912288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481034
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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