A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195111



Internal ID20762151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114156480..114168229hg38UCSC Ensembl
chr13:114921955..114933704hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3811750
hg1911750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482627
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195111
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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