A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479035



Internal ID256574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98128829..98129649hg38UCSC Ensembl
chr8:99141057..99141877hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014212
Samples
Known GenesPOP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479035
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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