A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986284



Internal ID20553325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106426352..106467111hg38UCSC Ensembl
chr11:106297079..106337838hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3840760
hg1940760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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