A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11661n54



Internal ID22779556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143125117..143200731hg38UCSC Ensembl
chr7:142822210..142897824hg19UCSC Ensembl
chr7:142532332..142607946hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3875615
hg1975615
hg1875615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608679, nsv608659, nsv608665, nsv608668
Samples
Known GenesPIP, TAS2R39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11661n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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