A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190130



Internal ID20757170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33699101..33721880hg38UCSC Ensembl
chr11:33720647..33743426hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3822780
hg1922780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473150
Supporting Variants
Samples
Known GenesC11orf91, CD59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190130
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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