A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478785



Internal ID256332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27499806..27509485hg38UCSC Ensembl
chr9:27499804..27509483hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg389680
hg199680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020204
Samples
Known GenesMOB3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478785
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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