A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484186



Internal ID261605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107891822..107916206hg38UCSC Ensembl
chr8:108904050..108928434hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3824385
hg1924385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014456
Samples
Known GenesRSPO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484186
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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