A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1069e199



Internal ID22758842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2567861..2571694hg38UCSC Ensembl
chr6:2568095..2571928hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg383834
hg193834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666264, esv2656698
SamplesHG00096, NA19701, NA11830, NA19700, NA19397, NA18924, HG01462, NA19909, NA20766, NA20508, NA19204, NA18508, NA19399, NA19332, HG01389, NA18917, HG00318, NA19359, NA19819, NA19393, NA18504, NA20332, NA20517, NA12400, HG01051, NA18510, HG01140, NA20814, NA07346, NA19374, NA19396, NA19381, NA19379, NA18519, HG01366, HG00122, NA18489, NA19448, NA19131, NA18916, NA11918, NA07347, NA19313, NA19138, NA18498, NA19904, NA19384, NA12761, NA19383, NA18874, HG00236, HG01072, NA19372, NA19385, HG00118, NA19189, NA19209, NA19789, NA19200, HG00739, HG01353, HG00137, HG00188, NA19707, NA19403, HG00245, NA18933, NA19391, NA19327, NA19236, NA20344, NA19654, NA18499, HG01383, NA19453, NA18912, NA19761, HG00146, NA19225, NA18523, NA19318, NA20799, NA20801, NA18909, NA19712, NA19435, NA19444, NA19380, NA19835, NA19334, NA19439, NA19428, NA19324, NA19311, HG01137, HG00116, HG01108, NA07037, HG00256, NA19376, NA19248, NA20582, NA19474, HG01055, NA18873, NA19116, NA18511, HG00553
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1069e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss108
Observed Complex0
Frequencyn/a


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