A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582691



Internal ID21531205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108223721..108225926hg38UCSC Ensembl
chr8:109235950..109238155hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382206
hg192206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140939
SamplesNA19239
Known GenesEIF3E
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582691
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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