A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489826



Internal ID267098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30522161..30646696hg38UCSC Ensembl
chr9:30522159..30646694hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38124536
hg19124536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489826
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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