A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5412220



Internal ID191524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128276997..128277048hg38UCSC Ensembl
chr10:130075261..130075312hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5412220
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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