A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482922



Internal ID260367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26265275..26427208hg38UCSC Ensembl
chr9:26265273..26427206hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38161934
hg19161934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482922
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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