A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561764



Internal ID22430532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59830179..59830179hg38UCSC Ensembl
chr20:58405234..58405234hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301054, nssv14301055
SamplesNA19239, NA19240
Known GenesPHACTR3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561764
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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