A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033807



Internal ID21943150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23453401..23454880hg38UCSC Ensembl
chr16:23464722..23466201hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381480
hg191480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033807
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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