A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485887



Internal ID263268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124252000..124266222hg38UCSC Ensembl
chr8:125264241..125278463hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3814223
hg1914223
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17017084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485887
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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