A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11660n54



Internal ID20145084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143095565..143239150hg38UCSC Ensembl
chr7:142792658..142936243hg19UCSC Ensembl
chr7:142502780..142646365hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38143586
hg19143586
hg18143586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608658, nsv608673
Samples
Known GenesPIP, TAS2R39, TAS2R40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11660n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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