A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636422



Internal ID21828469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5268309..5280792hg38UCSC Ensembl
chr20:5248955..5261438hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3812484
hg1912484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636422
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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