A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666343



Internal ID9932448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195272776..195272940hg38UCSC Ensembl
chr3:194993505..194993669hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5623334, essv6242128, essv5605237, essv6019639, essv6428544, essv6320702, essv5689520, essv5559354, essv5799953, essv6290004, essv6276353, essv5469373, essv5548815, essv6183372, essv5991613, essv6076393, essv5940362, essv6450949, essv6394638, essv6123582, essv6157701, essv6435228, essv5976280, essv5870023, essv5841010, essv6236381, essv6163451, essv6037755, essv5520795, essv6358617, essv5715635, essv5875134, essv5784017, essv5403280, essv6179824, essv6043543, essv6500747, essv5490312, essv5526114, essv5443597, essv5884462, essv5785700, essv5888735, essv6113370, essv5947767, essv6263851, essv5611365, essv5780959, essv5889061, essv6476852, essv6343767, essv6579017, essv6317133, essv6255746, essv6580620, essv5734168, essv6031975, essv6080458, essv6336660, essv5613070, essv5689007, essv5511649, essv5908812, essv5718700, essv5653619, essv5423171, essv6141262, essv5603643, essv6397999, essv5792762, essv5516398, essv6193658, essv5607996, essv6145847, essv5948427, essv5848161, essv5571484, essv5923538, essv6135474, essv5432993, essv5867513, essv6521514, essv6486322, essv6112398, essv6548386, essv5536610, essv5487805, essv6076749, essv5753711, essv6433645, essv6272271, essv6399542, essv5557534, essv6472665, essv6316382, essv5533499, essv6556983, essv6448165, essv5499772, essv6265857, essv5981480, essv6180520, essv5437089, essv6540404, essv5887257, essv6331886, essv6202963, essv5748571, essv6160131, essv6461211, essv5611450, essv6413416, essv6420357, essv5499763, essv5569070, essv6465107, essv5693448, essv5968261, essv5450464, essv5924228, essv6132374, essv5775350, essv5618357, essv5801054, essv5512776, essv5645750, essv5965585, essv5721175, essv6324881, essv5871119, essv5798151, essv5955888, essv6172537, essv5771094, essv6248610, essv5837077, essv6497769, essv6511328, essv5645169, essv6506268, essv5512255, essv5786985, essv5757306, essv6313186, essv6162501, essv6388229, essv5619842
SamplesHG01060, HG01441, HG00650, HG00542, HG00442, HG01173, HG01356, HG00536, NA19397, NA18621, HG00671, HG00524, NA18599, HG01389, HG01066, NA19359, HG00699, NA18596, NA19377, NA18530, NA18606, HG00449, HG00654, NA18602, HG00693, HG00271, HG00663, NA19396, NA19381, HG01350, NA18550, HG01366, HG00589, NA19382, NA18597, HG01351, HG00702, HG00689, HG00448, NA18635, HG00330, HG01083, HG01365, HG00334, HG00537, HG00590, HG00512, HG00281, HG00277, HG01069, HG00683, HG01170, NA18977, HG00325, HG01072, NA19371, HG00534, NA19385, HG00422, HG00705, NA18557, HG00419, HG00464, HG00108, HG00260, HG00543, HG01136, HG00154, NA18544, NA18613, HG00629, HG00443, HG00596, NA19403, HG00557, HG00428, HG00653, HG00701, HG00657, HG00475, HG00436, HG00556, HG00320, HG00584, HG00533, HG00583, NA18637, NA18534, HG00619, HG00708, HG00692, HG01390, HG00324, HG01073, HG00651, HG00690, HG00531, HG00479, HG00684, HG01101, HG00613, HG00525, HG01334, NA19009, HG00704, HG00463, NA18536, NA18634, HG01107, NA19401, NA18542, NA18543, NA18559, HG00353, HG00580, HG00375, HG00136, HG00278, HG01375, HG00473, HG00607, HG01108, NA19360, HG00256, HG00662, NA18610, HG00620, NA19376, HG00707, HG00672, HG00614, HG00513, HG00421, HG00329, HG00656, NA18636, HG00186, HG00280, HG01377, HG00472, NA18623, NA18549, HG01437, HG00437, HG00581, NA18577, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666343
Frequency
Sample Size1151
Observed Gain0
Observed Loss147
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer