A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601223



Internal ID16388632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29338679..29373531hg38UCSC Ensembl
Innerchr6:29306456..29341308hg19UCSC Ensembl
Innerchr6:29414435..29449287hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3834853
hg1934853
hg1834853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051669
Samples
Known GenesOR12D3, OR5V1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601223
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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