A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216210



Internal ID22362278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:20115914..20137605hg38UCSC Ensembl
Outerchr20:20096558..20118249hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3821692
hg1921692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14266632
SamplesNA19238
Known GenesC20orf26
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216210
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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