A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475019



Internal ID252665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35495000..35546000hg38UCSC Ensembl
chr9:35494997..35545997hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3851001
hg1951001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022502
Samples
Known GenesRUSC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475019
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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