A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489080



Internal ID266370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119616492..119616580hg38UCSC Ensembl
chr9:122378770..122378858hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489080
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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