A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568489



Internal ID21516838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20739738..20743351hg38UCSC Ensembl
chr8:20597249..20600862hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383614
hg193614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156018
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568489
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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