A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448416



Internal ID21105969
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 StatusM
Merged Variants
Supporting Variantsnssv18180864
Samples
Known GenesOR51B2, OR51B5, OR51B6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448416
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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