A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3534748



Internal ID22404023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34200958..34201024hg38UCSC Ensembl
chr20:32788764..32788830hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5248n152
Supporting Variantsnssv14299889, nssv14299890
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3534748
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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