A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562354



Internal ID22431108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39326085..39326085hg38UCSC Ensembl
chr20:37954728..37954728hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14300715, nssv14300716, nssv14300719, nssv14300717, nssv14300718, nssv14300720
SamplesHG00512, NA19238, HG00732, NA19240, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562354
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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