A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533115



Internal ID309013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89676194..89678013hg38UCSC Ensembl
chr15:90219425..90221244hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381820
hg191820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704136
Samples
Known GenesPLIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533115
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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