A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667320



Internal ID9933425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41311822..41312232hg38UCSC Ensembl
chr15:41604020..41604430hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6480175, essv5856961, essv5608150, essv6019189, essv5672400, essv5417439, essv6460714, essv5670418, essv6294720, essv5988342, essv5712329, essv5438944, essv6153150, essv5441422, essv5446309, essv6571851, essv6474754, essv6274001, essv5680987, essv6566513, essv6380427, essv5902922, essv5395612, essv6472135, essv6046651, essv5891297, essv6160726, essv5543462, essv6473015, essv6392437, essv5627849, essv5979038, essv6326055, essv5987927, essv5606077, essv6063821, essv5399324, essv5957219, essv6487797, essv6461081, essv5589917, essv6010190, essv5714702, essv5924930, essv6574917, essv6267916, essv6279318, essv5590308, essv6306040, essv6235873, essv6255324, essv5893991, essv5730726, essv5781473, essv5647015, essv6258688, essv6370318, essv5483513, essv5794191, essv6368006, essv5713122, essv6499683, essv6477698, essv5789565, essv5846054, essv5833740, essv6213195, essv5419086, essv6553154, essv5873455, essv6448587, essv6047145, essv6429322, essv6290487, essv5843867, essv5430851, essv6288111, essv5400203, essv6247815, essv6249606, essv6019017, essv6526362, essv6363641, essv5553514, essv6436956, essv5635297, essv5846990, essv5845915, essv6449719, essv5897218, essv5971319, essv5400093, essv6190625, essv5610450, essv6553466, essv5531919, essv6011460, essv6105500, essv5524720, essv6001061, essv6472456, essv5740202, essv6394776, essv5952977, essv5498029, essv6120749, essv5561448, essv6588803, essv5706240, essv5452339, essv6550160, essv5604385, essv6132740, essv6409227, essv6272332, essv6020101, essv6439317, essv6161588, essv5552174, essv5445724, essv6542777, essv5878518, essv5977962, essv6095184, essv5636005, essv6564066, essv6244486, essv6244354, essv6225903, essv5915240, essv5751785, essv5702716, essv6484074, essv5887047, essv6001806, essv6497711, essv6250387, essv6027139, essv6259306, essv6291468, essv6584754, essv5704107, essv6511985, essv5671737, essv5845966, essv6467573, essv6433975, essv5877337, essv6041152, essv5464440, essv5887942, essv6274879, essv6156661, essv6036766, essv5998319, essv5846177, essv5743709, essv5450960, essv5843953, essv6595313, essv5928427, essv5891398, essv6295388, essv6582436, essv5833552, essv6468752, essv5839988, essv6552626, essv5830558, essv6239051, essv6231564, essv5913485, essv5990413, essv5610616
SamplesHG00096, NA11830, NA12842, HG01356, HG01462, NA11995, HG00242, NA18508, HG01052, NA19704, HG01389, HG00315, HG00151, NA20816, NA20813, HG00233, NA12045, HG00640, HG00244, NA12004, NA20805, NA19684, NA20808, NA20507, HG01461, NA12399, NA20806, HG01140, HG00337, HG00138, NA19171, HG01350, NA20796, HG00272, NA19201, NA20798, NA20589, HG01351, NA19678, HG00173, NA20774, NA20756, HG01492, NA19131, HG00369, HG00270, NA19681, NA18949, HG00158, NA20541, HG01134, HG00281, HG00139, NA20759, HG00277, NA12275, HG01080, HG00335, HG00106, NA20819, NA12156, NA06984, HG00156, NA11932, HG01072, NA12044, NA11994, NA19207, HG00309, HG00118, HG01198, HG00637, HG01048, HG01133, NA12828, NA20533, HG00323, HG01550, HG00253, NA20755, HG00264, HG00108, HG01353, HG00133, NA12777, HG01183, HG01136, HG00188, NA19657, HG00183, HG00176, HG01171, HG01384, HG00328, HG00245, NA19152, NA12878, HG00732, HG00344, NA20506, NA20519, NA19658, NA18976, NA20770, NA19776, HG00740, HG00324, HG00284, NA11919, HG00373, HG00479, NA20581, NA12892, HG00117, HG00140, HG00152, NA20828, NA19756, HG00126, NA12546, HG01107, NA19675, NA20765, NA18608, NA18953, NA20799, NA19652, HG00155, HG00254, HG00285, NA18952, NA12775, HG00357, NA19144, NA20785, HG01357, HG00308, NA20778, HG00237, HG00319, NA12763, HG01489, HG00339, HG00269, HG00125, HG00111, HG00259, NA20582, HG00342, NA19716, HG00267, HG01055, NA20510, HG00112, NA20807, NA11843, NA20826, NA19780, HG00343, NA20528, HG00252, NA20503, NA19661, NA20502, HG01125, HG00345, NA18511, NA12154, HG01112, HG00554, HG00180, HG01437, NA18562, NA12776
Known GenesOIP5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667320
Frequency
Sample Size1151
Observed Gain0
Observed Loss174
Observed Complex0
Frequencyn/a


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