A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765694



Internal ID20541554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59821974..59821974hg38UCSC Ensembl
chr20:58397029..58397029hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291234
Samples
Known GenesPHACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765694
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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