A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211282



Internal ID20778322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98138513..98369776hg38UCSC Ensembl
chr3:97857357..98088620hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38231264
hg19231264
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375576
Supporting Variants
Samples
Known GenesOR5H14, OR5H15, OR5H2, OR5H6, OR5K4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211282
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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