A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485329



Internal ID262721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113855911..113855984hg38UCSC Ensembl
chr9:116618191..116618264hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485329
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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