A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561870



Internal ID22430638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23334204..23334204hg38UCSC Ensembl
chr20:23314841..23314841hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14297700, nssv14297699
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561870
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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