A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194003



Internal ID20761043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26249196..26258028hg38UCSC Ensembl
chr18:23829160..23837992hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg388833
hg198833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534640
Supporting Variants
Samples
Known GenesTAF4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194003
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00033


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