A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1039n223



Internal ID22804007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47972248..48796499hg38UCSC Ensembl
chr11:47993800..48818051hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38824252
hg19824252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6459403, nsv6455948
Samples
Known GenesOR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1039n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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