A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486485



Internal ID263850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116273272..116293241hg38UCSC Ensembl
chr8:117285505..117305476hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3819970
hg1919972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17017950
Samples
Known GenesLINC00536
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486485
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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