A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665954



Internal ID9932059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23234669..23235625hg38UCSC Ensembl
chr22:23576856..23577812hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5865104, essv5650363, essv5459501, essv6024593, essv6356211, essv6237681, essv5867300, essv5684865, essv5760205, essv5984051, essv5857855, essv6045451, essv5558537, essv6249269, essv6092601, essv5588787, essv6559707, essv5776995, essv5583122, essv6105091, essv6577807, essv6290012, essv5977228, essv6458272, essv6414317, essv5966151, essv5802203, essv5676330, essv6286541, essv6003489, essv5608373, essv5452355, essv6427696, essv5626716, essv6129734, essv6236704, essv6384592, essv6477254, essv6376875, essv5783634, essv5428193, essv5727794, essv5467830, essv6173772, essv5443739, essv6099426, essv5489412, essv6115646, essv5699419, essv5546622, essv6003867, essv6226161, essv5870143, essv6306744, essv5546784, essv6184941, essv6174755, essv5422258, essv6407259, essv5858622, essv6402539, essv6304538, essv6013586, essv6311131, essv5819874, essv5977722, essv5775505, essv5797690, essv5496994, essv6518489, essv6082887, essv5430006, essv6225784, essv6008982, essv5841032, essv5522820, essv6127165, essv5493767, essv5662615, essv5601814, essv5541153, essv5893678, essv5900616, essv6379123, essv6271675, essv5834139, essv6198584, essv5497305, essv6186912, essv5657351, essv5506921, essv6351881, essv5709451, essv5690732, essv6576469, essv6398003, essv6087962, essv5791032, essv6349611, essv5721297, essv6509726, essv6579389, essv6571101, essv6413548, essv6344871, essv6137700, essv6375234, essv6389999, essv6033767, essv6187287, essv5517088, essv6589555, essv5497241, essv6498691, essv5748581, essv5478511, essv6076910, essv5773672, essv5877497, essv5527966, essv5515945, essv5401872, essv6241108, essv5696669, essv5597975, essv6488397, essv6027001, essv5868634, essv6241698, essv6036895, essv5515187, essv6398497, essv6298007, essv6012699, essv6421498, essv5882370, essv5681146, essv5505992, essv6333459, essv6485933, essv6353540, essv6216048, essv5500939, essv6301096, essv6258589, essv6447745, essv6338402, essv5777120, essv5676525, essv6466060, essv5466945, essv6230516, essv6055771, essv5842367, essv6342423, essv5987627, essv5902297, essv5592092, essv5455833, essv6133051, essv5750498, essv5516185, essv5969558, essv5490875, essv5757913, essv6329646, essv6285711, essv5485543, essv6322578, essv5868793, essv5634343, essv6263565, essv5989943, essv5820598, essv6146252, essv6053359, essv6276172, essv6098159, essv5983984, essv5541834, essv6466732, essv6184049, essv5453436, essv6202436, essv5972892, essv5436817, essv5517518, essv6470801, essv6248491, essv5409296, essv5590263, essv5567286, essv6260856, essv6580523, essv6498535, essv5995113, essv5553759, essv6379259, essv5614121, essv6206357, essv5475167, essv5407994, essv5687722, essv6165995, essv6003979, essv5488041, essv6272458, essv6282622, essv6020315, essv5463499, essv5923916, essv5457192, essv5957842, essv5904368, essv5713519, essv5493356, essv5551562, essv5672389, essv5685734, essv6592353, essv5808440, essv5611469
SamplesNA19463, NA18549, HG01437, NA12776, NA20509, NA20588, NA12383, HG01060, HG00114, NA19648, HG01098, HG01356, NA20543, HG00231, NA18947, NA12286, HG00249, NA11829, HG01359, HG01052, HG00187, NA20783, NA12414, HG00100, NA12843, NA20531, NA11931, NA18599, HG01389, HG01374, HG00151, NA20816, NA20813, NA20802, NA12045, HG00640, HG00367, HG00699, NA18545, NA19393, NA12340, HG00177, HG00150, NA20507, NA12400, HG00261, NA20771, NA20806, NA12413, NA20814, NA07346, HG00641, NA19746, HG00138, NA19660, HG01350, NA20796, NA18550, HG00589, HG00272, HG00251, HG00122, NA20798, NA20589, HG00448, NA20586, HG00173, NA20774, HG01168, NA20756, NA20769, NA12348, HG01492, HG00736, NA11992, NA11918, NA07347, HG00346, NA20768, HG00247, HG00369, HG01365, HG00311, NA12761, NA11930, HG01134, NA20539, HG00277, HG01455, HG01069, NA19651, HG00120, HG00335, HG00148, NA20819, NA12156, HG00236, NA20812, NA19719, HG00232, HG00422, HG01176, NA18986, NA12889, HG00309, NA19002, HG00637, NA12828, HG00326, HG00178, NA20757, NA20533, HG00253, NA20515, HG00739, HG00264, NA11993, HG01124, HG00260, NA20818, HG00137, HG01136, HG00188, NA20535, HG00176, HG01171, HG00282, NA19670, HG01384, NA12003, HG00190, NA20810, HG00344, HG01498, NA19658, NA20770, HG00551, NA18537, NA20525, HG00324, NA19655, HG00373, NA11893, NA11894, NA20538, NA12249, NA19453, HG01101, HG00157, HG01497, NA19338, HG00276, HG00146, NA19682, NA12144, NA18523, HG00463, NA20534, HG01204, NA19436, NA20765, NA12043, NA20296, HG00258, NA20799, NA19729, NA20522, NA20801, NA11881, HG00336, HG00285, HG00265, NA19434, NA12775, HG00353, HG01551, HG00136, NA20804, NA07051, NA20785, HG01174, NA20527, HG00308, NA20792, NA20778, HG00237, NA19679, NA20504, HG00319, HG00116, NA20516, NA20803, NA07037, HG01489, HG00339, HG00269, NA19759, NA18501, HG00111, HG00478, HG01491, HG00259, NA20582, HG00329, HG00123, NA12830, HG00112, NA20807, HG00280, HG00131, NA11843, NA19780, HG00343, NA20528, NA18983, HG01251, HG00377, HG00252, NA19661, NA07056, HG01378, HG01125
Known GenesBCR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665954
Frequency
Sample Size1151
Observed Gain0
Observed Loss222
Observed Complex0
Frequencyn/a


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