A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476899



Internal ID254498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84515893..84528878hg38UCSC Ensembl
chr8:85428128..85441113hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3812986
hg1912986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015412
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476899
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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