A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561862



Internal ID22430630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11009487..11009487hg38UCSC Ensembl
chr20:10990135..10990135hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14298682, nssv14298683, nssv14298684
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561862
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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