A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182082



Internal ID20749122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103943594..103967239hg38UCSC Ensembl
chr14:104409931..104433576hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3823646
hg1923646
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501238
Supporting Variants
Samples
Known GenesTDRD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182082
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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