A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481401



Internal ID258881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40023031..40043473hg38UCSC Ensembl
chr8:39880550..39900992hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3820443
hg1920443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481401
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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