A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664253



Internal ID21612558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64843579..64843579hg38UCSC Ensembl
chr15:65135778..65135778hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090173
SamplesHG01596
Known GenesPLEKHO2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664253
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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