A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474022



Internal ID251694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70688212..70688295hg38UCSC Ensembl
chr9:73303128..73303211hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023320
Samples
Known GenesTRPM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474022
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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