A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272501



Internal ID20481719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90020806..90020806hg38UCSC Ensembl
chr14:90487150..90487150hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765163
Supporting Variants
Samples
Known GenesTDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272501
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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