A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187245



Internal ID20754285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47199803..47205871hg38UCSC Ensembl
chr11:47221354..47227422hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg386069
hg196069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187245
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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