A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090173



Internal ID21452176
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 StatusS
Merged Variantsnsv5664253
Supporting Variants
SamplesHG01596
Known GenesPLEKHO2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090173
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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