A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281553



Internal ID20490771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60721394..60730285hg38UCSC Ensembl
chr20:59296452..59305343hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg388892
hg198892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746337
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281553
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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