A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481234



Internal ID258722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109074475..109075719hg38UCSC Ensembl
chr8:110086704..110087948hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481234
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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