A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043473



Internal ID21952777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16056090..16056215hg38UCSC Ensembl
chr20:16036735..16036860hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632684
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043473
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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