A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476058



Internal ID253680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90098812..90098992hg38UCSC Ensembl
chr9:92861094..92861274hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476058
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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