A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566298



Internal ID21514622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84310752..84311086hg38UCSC Ensembl
chr8:85222987..85223321hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158645
SamplesNA19239
Known GenesRALYL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566298
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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