A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489109



Internal ID266398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53844291..53845273hg38UCSC Ensembl
chr8:54756851..54757833hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38983
hg19983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489109
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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