A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363139



Internal ID21020692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98215695..98266376hg38UCSC Ensembl
chr3:97934539..97985220hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3850682
hg1950682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211287
Samples
Known GenesOR5H6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363139
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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