A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517466



Internal ID293887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67115609..67115662hg38UCSC Ensembl
chr15:67407947..67408000hg19UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702906
Samples
Known GenesSMAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517466
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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