A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1625n54



Internal ID22769520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6723715..6786012hg38UCSC Ensembl
chr11:6744946..6807243hg19UCSC Ensembl
chr11:6701522..6763819hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3862298
hg1962298
hg1862298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553376, nsv553375
Samples
Known GenesOR2AG1, OR2AG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1625n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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