A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492513



Internal ID269723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107225108..107225256hg38UCSC Ensembl
chr9:109987389..109987537hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028234
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492513
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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