A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205261



Internal ID20772301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19884360..19894089hg38UCSC Ensembl
chr20:19865004..19874733hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg389730
hg199730
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532919
Supporting Variants
Samples
Known GenesRIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205261
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00036


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