A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv82n21



Internal ID18990555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123901052..124289279hg38UCSC Ensembl
chr11:123771759..124159175hg19UCSC Ensembl
chr11:123276969..123664385hg18UCSC Ensembl
chr11:123276969..123664385hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38388228
hg19387417
hg18387417
hg17387417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527167, nsv525021
Samples
Known GenesOR10G4, OR10G7, OR10G8, OR10G9, OR10S1, OR4D5, OR6T1, OR8D4, OR8G1, OR8G2, OR8G5, VWA5A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv82n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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