A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397980



Internal ID177380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140544522..140544573hg38UCSC Ensembl
chr3:140263364..140263415hg19UCSC Ensembl
Cytoband3q23
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 Variantsnssv16939379
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397980
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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