A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5410389



Internal ID189704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20086284..20086335hg38UCSC Ensembl
chr1:20412777..20412828hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901011
Samples
Known GenesPLA2G5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5410389
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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