A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3531480



Internal ID22400833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34129740..34129816hg38UCSC Ensembl
chr20:32717546..32717622hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299885
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3531480
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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