A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276511



Internal ID20485729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98540520..98540654hg38UCSC Ensembl
chr12:98934298..98934432hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733565
Supporting Variants
Samples
Known GenesTMPO
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276511
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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