A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485298



Internal ID262692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33044482..33044970hg38UCSC Ensembl
chr9:33044480..33044968hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023497
Samples
Known GenesSMU1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485298
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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