A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409192



Internal ID188514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87914770..87914770hg38UCSC Ensembl
chr10:89674527..89674527hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038399
Samples
Known GenesPTEN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409192
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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