A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478904



Internal ID256448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15488841..15489517hg38UCSC Ensembl
chr9:15488839..15489515hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020614
Samples
Known GenesPSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478904
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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