A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486185



Internal ID263557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13720426..13738989hg38UCSC Ensembl
chr9:13720425..13738988hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3818564
hg1918564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486185
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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