A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480565



Internal ID258071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93470222..93487000hg38UCSC Ensembl
chr8:94482450..94499228hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3816779
hg1916779
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013557
Samples
Known GenesLINC00535
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480565
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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