A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185303



Internal ID20752343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2187955..2203542hg38UCSC Ensembl
chr11:2209185..2224772hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3815588
hg1915588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443956
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185303
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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