A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020539



Internal ID21929882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58253568..58261771hg38UCSC Ensembl
chr16:58287472..58295675hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg388204
hg198204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635068
Samples
Known GenesCCDC113
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020539
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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