A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667791



Internal ID21616096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59821975..59821975hg38UCSC Ensembl
chr20:58397030..58397030hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117508
SamplesNA19239
Known GenesPHACTR3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667791
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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