A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220052



Internal ID22364872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35568617..35569219hg38UCSC Ensembl
chr20:34156536..34157149hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38603
hg19614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299966
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220052
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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