A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431373



Internal ID210151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59688519..59688570hg38UCSC Ensembl
chr15:59980718..59980769hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700980
Samples
Known GenesBNIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431373
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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