A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698074



Internal ID21219928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107590334..107590389hg38UCSC Ensembl
chr11:107461060..107461115hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698074
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.733333


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