A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489186



Internal ID266474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128290811..128291948hg38UCSC Ensembl
chr9:131053090..131054227hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381138
hg191138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489186
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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