A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181718



Internal ID20748758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118990788..118992749hg38UCSC Ensembl
chr11:118861498..118863459hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381962
hg191962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00061


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