A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv45e199



Internal ID20123347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61647741..61654470hg38UCSC Ensembl
chr1:62113413..62120142hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg386730
hg196730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2667857, esv2657809
SamplesHG00323, HG00613, NA19248, NA12718, HG00537, HG01359, NA12249, HG00252, HG00318, HG00607, HG01440, NA07347, NA12750, HG00257, NA18595, NA20771, HG00182, NA07037, NA18951, HG00619, HG01250, HG01072, HG01519, NA12286, HG00100, NA19081, HG00127, HG00328, HG01055, HG00705, HG00437, HG00464, HG00596, HG00131, NA20796, NA18526, HG00155, NA20508, HG00160, HG00449, HG00261, HG01098, HG01079, NA18603, NA20802, NA18948, NA19670, HG00463, HG01051, NA12813, HG00117, HG00577, HG01082, HG00475, HG01174, NA19920, HG00190, HG00122, NA18546, HG00106, HG00698, NA20588, HG00111, HG00334, NA12776, NA19685, HG00187, HG01461, NA19648, NA20314, HG01134, HG01168, HG00366, HG00177, HG00331, HG00146, NA18965, HG00319, NA12341, NA12287, NA18950, HG00554, HG01133, HG00592, HG00115, HG00154, NA18559, HG00321, HG00339, HG01550, HG00158, NA20585, NA19982, HG00346, HG01456, NA18627, HG01375, NA19652, NA12383, HG00337, NA18635, NA19068, NA18536, NA12155, HG00259, HG00096, NA07357, HG01048, HG01061, HG01124, HG00330, NA18959, HG00150, HG00533, NA18609, HG00178, HG00419, HG00258, NA11831, HG01113, NA18637, NA19835, HG00174, HG00634, HG00637, NA18593, NA19681, HG00243, NA19663, HG01187, HG00237, HG00584, NA19684, NA20773, HG00114, NA12751, NA19676, HG00436, HG00620, NA19786, HG01097, NA19785, HG00268, HG01066, NA20348, HG00732, HG00325, HG00185, NA20753, HG01455, NA19005, HG00560, HG01073, NA18558, NA19664, HG00672, HG01069, HG01176, NA19704, NA18961, HG00103, HG01080, NA20815, HG00740, NA18613, NA20797, HG00524, HG01494, NA20582, NA19720, HG00329, HG00512, HG00534, HG01060, HG01383, HG00236, HG00589, NA18606, NA19777, HG01094, NA18619, NA18987, NA18999, NA20537, HG00595, HG01190, NA19729, NA12272, NA18599, NA18567, NA19078, HG01334, NA19009, HG00663, NA12889, NA19747, HG00448, NA18602, NA19755, NA20317, NA11830, NA12003, HG00123, NA19749, NA12399, NA19717, NA12842, NA19655, HG01366, NA19732, HG00422, NA20543, HG00708, HG01108, NA18610, HG01251, HG00367, NA11932, HG00566, HG01125, NA11829, HG00119, HG00324, HG00625, HG00690, NA20528, HG00641, NA18549, NA18574, HG01102, HG01377, HG00476, NA20502, NA19087, NA19750, NA19661, NA19779, NA19058
Known GenesMGC34796
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv45e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss238
Observed Complex0
Frequencyn/a


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