A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210418



Internal ID22358329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16894228..16894385hg38UCSC Ensembl
chr20:16874873..16875030hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14296877
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210418
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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