A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv45e199

Internal ID20123347
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61647741..61654470hg38UCSC Ensembl
chr1:62113413..62120142hg19UCSC Ensembl
Allele length
AssemblyAllele length
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
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)dgv45e199
Sample Size1151
Observed Gain0
Observed Loss238
Observed Complex0

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