A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561876



Internal ID22430644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40298243..40298243hg38UCSC Ensembl
chr20:38926883..38926883hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14300766, nssv14300765
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561876
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer