A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5402015



Internal ID181388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32885017..32885017hg38UCSC Ensembl
chr8:32742535..32742535hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5402015
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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