A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481059



Internal ID258554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38082025..38091759hg38UCSC Ensembl
chr8:37939543..37949277hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg389735
hg199735
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17010637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481059
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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