A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218386



Internal ID22363742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35906443..35906535hg38UCSC Ensembl
chr20:34494365..34494457hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5255n152
Supporting Variantsnssv14300597, nssv14300596
SamplesHG00732, HG00733
Known GenesPHF20
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218386
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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