A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029071



Internal ID21938414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23643248..23645191hg38UCSC Ensembl
chr16:23654569..23656512hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381944
hg191944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605289
Samples
Known GenesDCTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029071
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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