A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733393



Internal ID20509322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79617679..79617744hg38UCSC Ensembl
chr16:79651576..79651641hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733393
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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