A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482669



Internal ID260120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37754025..37754092hg38UCSC Ensembl
chr9:37754022..37754089hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024779
Samples
Known GenesTRMT10B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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