A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094782



Internal ID21500813
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 StatusS
Merged Variantsnsv5665169
Supporting Variants
SamplesNA19239
Known GenesPLCB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094782
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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