A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5398260



Internal ID177658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125663876..125663885hg38UCSC Ensembl
chr8:126676120..126676129hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17016336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5398260
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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