A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484856



Internal ID262259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106057396..106063732hg38UCSC Ensembl
chr8:107069624..107075960hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg386337
hg196337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484856
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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