A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621461



Internal ID21813508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25715673..25727411hg38UCSC Ensembl
chr20:25696309..25708047hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3811739
hg1911739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621461
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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