A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180864



Internal ID20747904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5315096..5363305hg38UCSC Ensembl
chr11:5336326..5384535hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3848210
hg1948210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448416
Supporting Variants
Samples
Known GenesOR51B2, OR51B5, OR51B6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180864
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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