A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029552



Internal ID21938895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78827909..78894059hg38UCSC Ensembl
chr16:78861806..78927956hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3866151
hg1966151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620770
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029552
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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