A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194257



Internal ID20761297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13232202..13255048hg38UCSC Ensembl
chr11:13253749..13276595hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3822847
hg1922847
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194257
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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