A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561881



Internal ID22430649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51211008..51211008hg38UCSC Ensembl
chr20:49827545..49827545hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299502, nssv14299503
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561881
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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