A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490080



Internal ID267343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6133991..6237755hg38UCSC Ensembl
chr9:6133991..6237755hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38103765
hg19103765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020411
Samples
Known GenesIL33
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490080
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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