A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478644



Internal ID256193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14520007..14520069hg38UCSC Ensembl
chr9:14520005..14520067hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17019099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478644
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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