A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480959



Internal ID258455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35175838..35176369hg38UCSC Ensembl
chr9:35175835..35176366hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021548
Samples
Known GenesUNC13B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480959
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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