A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11668n54



Internal ID22779563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144190093..144379671hg38UCSC Ensembl
chr7:143887186..144076764hg19UCSC Ensembl
chr7:143518119..143707697hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38189579
hg19189579
hg18189579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608750, nsv608729, nsv608705, nsv608717, nsv608742, nsv608718, nsv608726, nsv608713, nsv608734, nsv608756, nsv608728, nsv608711, nsv608709, nsv608739, nsv608769, nsv608733, nsv608738, nsv608706, nsv608707, nsv608735, nsv608704, nsv608720, nsv608716, nsv608747, nsv608743, nsv608731, nsv608727, nsv608725, nsv608719, nsv608746, nsv608737, nsv608745, nsv608740, nsv608736, nsv608708, nsv608732, nsv608715, nsv608710, nsv608755, nsv608748, nsv608791, nsv608749, nsv608724, nsv608744, nsv608730
Samples
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11668n54
Frequency
Sample Size17421
Observed Gain73
Observed Loss0
Observed Complex0
Frequencyn/a


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