A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733474



Internal ID20509404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98539079..98539140hg38UCSC Ensembl
chr12:98932857..98932918hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294061
Samples
Known GenesTMPO
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733474
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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