A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561879



Internal ID22430647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50666190..50666190hg38UCSC Ensembl
chr20:49282727..49282727hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299479, nssv14299478
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561879
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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