A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194417



Internal ID20761457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21336380..21359207hg38UCSC Ensembl
chr11:21357926..21380753hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822828
hg1922828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438300
Supporting Variants
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194417
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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