A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479807



Internal ID257323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102706163..102716201hg38UCSC Ensembl
chr8:103718391..103728429hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3810039
hg1910039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015812
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479807
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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