A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561866



Internal ID22430634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17778562..17778562hg38UCSC Ensembl
chr20:17759207..17759207hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14297538, nssv14297539, nssv14297540
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561866
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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