A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489664



Internal ID266937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11647634..11936210hg38UCSC Ensembl
chr9:11647634..11936210hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38288577
hg19288577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv523n206
Supporting Variantsnssv17022250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489664
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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