A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666656



Internal ID21614962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59822166..59822166hg38UCSC Ensembl
chr20:58397221..58397221hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117510
SamplesNA19983
Known GenesPHACTR3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666656
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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