A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276803



Internal ID20486021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34228126..34231423hg38UCSC Ensembl
chr20:32815932..32819229hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276803
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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