A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993498



Internal ID20560538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6758184..6872396hg38UCSC Ensembl
chr11:6779415..6893627hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38114213
hg19114213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443114
Supporting Variants
Samples
Known GenesOR10A2, OR10A5, OR2AG1, OR2AG2, OR6A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993498
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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