A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3533042



Internal ID22402359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32494920..32494975hg38UCSC Ensembl
chr20:31082723..31082778hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299841
SamplesNA19239
Known GenesC20orf112
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3533042
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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