A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483567



Internal ID261001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130639921..130655566hg38UCSC Ensembl
chr9:133515308..133530953hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3815646
hg1915646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483567
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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