A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665169



Internal ID21613474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40291941..40299299hg38UCSC Ensembl
chr15:40584142..40591500hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg387359
hg197359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094782
SamplesNA19239
Known GenesPLCB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665169
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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