A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv826e199



Internal ID22758599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23972056..23993698hg38UCSC Ensembl
chr22:24314245..24335892hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3821643
hg1921648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678821, esv2660107, esv2667759, esv2661400
SamplesHG00114, HG01441, NA19648, HG00143, HG00231, HG00249, NA11995, HG00361, HG00242, HG01359, NA12273, NA12414, HG00100, NA12843, NA11933, NA11931, HG00257, HG01389, HG00151, HG00233, NA12045, HG00318, HG00244, HG00181, HG00103, NA19777, NA12340, HG01456, HG00177, HG01461, HG00261, NA12399, NA12155, HG01140, NA12341, HG00337, HG00327, NA07346, HG00127, HG01350, HG00272, HG00122, NA19728, HG01351, HG01488, HG00173, NA19723, HG00330, NA12348, HG01492, NA11992, NA07048, NA11918, NA07347, HG00346, NA12287, HG00247, HG00369, HG00270, HG00334, NA19782, NA19681, HG00185, HG00243, HG00158, NA12761, HG00281, HG00139, NA12282, HG00277, NA12275, NA19651, HG00335, HG00106, NA12156, NA06984, HG00236, HG00156, HG00325, HG00232, HG00309, HG00118, NA19725, HG00338, HG00159, NA12828, HG00326, HG00323, HG00253, NA12748, HG00108, HG00260, NA11831, HG00137, NA12777, HG01136, HG00188, NA12489, NA19657, HG00268, HG00266, HG00183, HG00176, HG01384, HG00328, NA12342, NA12003, HG00368, NA19717, NA19663, HG00320, HG00344, HG01498, HG00263, NA19788, HG00275, NA12718, HG00239, NA19654, HG00324, HG00284, HG00273, NA11919, HG00250, NA19655, HG00373, NA11893, HG00331, NA11894, NA12249, HG00117, HG00321, HG00140, HG01334, NA19761, HG00152, NA19682, NA12144, HG00246, HG00126, HG01148, HG00258, NA19729, HG00124, NA19652, NA12716, HG00254, HG00119, NA11881, HG00336, HG00285, NA19747, HG00366, HG00375, NA19732, NA12272, NA12046, HG01375, HG00237, NA19679, HG00319, HG00256, NA12763, NA12347, NA06986, HG00339, HG00269, HG00125, HG00111, NA19785, HG01491, HG00329, NA19716, HG00267, HG01254, HG00174, HG00123, NA12830, HG00112, NA19770, HG00280, NA11843, NA19780, HG00343, HG01251, HG00377, HG00372, HG00274, HG00252, HG01378, HG01125, HG00171, NA12006, NA12154, HG01112, HG00180, HG01437, NA12776, NA19676
Known GenesDDT, DDTL, GSTT2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv826e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss199
Observed Complex0
Frequencyn/a


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