A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486520



Internal ID263884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107527768..107533275hg38UCSC Ensembl
chr9:110290049..110295556hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg385508
hg195508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486520
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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