A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521393



Internal ID297689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9111537..9135141hg38UCSC Ensembl
chr19:9222213..9245817hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3823605
hg1923605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721204
Samples
Known GenesOR7G1, OR7G3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521393
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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