A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410314



Internal ID189631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34528192..34528243hg38UCSC Ensembl
chr8:34385710..34385761hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410314
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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