A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291234



Internal ID20500452
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 StatusS
Merged Variantsnsv4765694
Supporting Variants
Samples
Known GenesPHACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291234
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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