A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv589n54



Internal ID20134013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158715246..158883163hg38UCSC Ensembl
chr1:158685036..158852953hg19UCSC Ensembl
chr1:156951660..157119577hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38167918
hg19167918
hg18167918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv547988, nsv547989
Samples
Known GenesMNDA, OR6K3, OR6K6, OR6N1, OR6N2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv589n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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