A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050356



Internal ID21959589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46788838..46789408hg38UCSC Ensembl
chr20:45417477..45418047hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050356
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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