A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989341



Internal ID20556381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21746984..21756076hg38UCSC Ensembl
chr11:21768530..21777622hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg389093
hg199093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443389
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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