A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3532427



Internal ID22401754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21209593..21209838hg38UCSC Ensembl
chr20:21190231..21190476hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14297620
SamplesNA19238
Known GenesPLK1S1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3532427
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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