A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664503



Internal ID9930608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27488703..27489081hg38UCSC Ensembl
chr3:27530194..27530572hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5728171, essv5651084, essv5742098, essv5423855, essv5395984, essv6394621, essv5602877, essv6113883, essv6096969, essv5980372, essv5517755, essv6379590, essv5650191, essv6006701, essv5766095, essv6346549, essv5968767, essv6352477, essv5458657, essv5918898, essv6107817, essv5728047, essv6409618, essv5993273, essv5920731, essv6076656, essv5632251, essv5716319, essv6524657, essv6077482, essv5947154, essv6353431, essv6521385, essv5789837, essv6307396, essv6536812, essv5489992, essv5510493, essv5395841, essv6051483, essv5564903, essv5926912, essv5423303, essv5888078, essv5879301, essv5837302, essv5499274, essv6090450, essv6200289, essv6215567, essv6214483, essv5668150, essv5464124, essv6216811, essv6367558, essv6118425, essv6329525, essv6271939, essv5804848, essv6249002, essv6021576, essv5626897, essv5454725, essv5715015, essv5637068, essv5481233, essv6352386, essv6296755, essv6234847, essv5816813, essv6526602, essv6389056, essv5492103, essv6110324, essv6051811, essv6033246, essv6021943, essv5712761, essv6120548, essv6486675, essv6476306, essv5944247, essv5931048, essv5614769, essv6035968, essv6094077, essv6425607, essv5405728, essv5485707, essv6112916, essv5532402, essv6255509, essv5910406, essv6176254, essv5983644, essv6392225, essv5819646, essv6377736, essv5561226, essv6203318, essv6517549, essv5710819, essv6054724, essv6419620, essv5944674, essv5545883, essv6063396, essv6137947, essv5916643, essv5998222, essv6005907, essv5944343, essv5760228, essv6593223, essv6145214, essv5477706, essv6164738, essv5773305, essv5487574, essv5871906, essv6020014, essv6425416, essv5721248
SamplesHG00403, NA20761, HG01521, NA12842, HG00143, NA19703, NA18924, HG01462, NA19664, HG01359, HG00524, HG01052, NA19332, NA18565, NA11933, HG01374, NA18917, NA19092, NA18486, HG01465, NA19819, NA19777, NA19684, NA18530, NA18606, HG00737, NA19920, NA12155, NA20806, HG01140, HG00271, NA19660, NA18519, NA19382, NA20798, HG01488, NA19916, HG00330, NA12348, HG01492, NA19197, NA12283, NA18498, NA19130, NA19404, NA19720, NA19651, HG01080, HG00120, HG00683, HG01170, NA18977, HG01495, HG00325, NA19372, HG00534, NA19172, NA19317, NA19901, NA18520, HG00338, HG01048, HG01133, NA18908, NA19985, HG01550, NA19789, HG00739, HG01353, HG00380, NA19707, NA19070, NA19077, NA19347, NA18956, NA19236, NA19982, NA18572, HG01047, HG01094, NA19655, HG00404, HG00531, NA20581, NA11893, HG01197, NA18499, HG01383, NA20282, NA18963, NA19436, NA20773, NA19256, NA18559, NA19473, HG00734, NA20804, NA19380, NA12046, HG01357, NA20790, NA19835, HG00237, NA19428, NA18943, NA20341, NA19248, NA19779, HG00267, NA18873, NA20807, NA11843, NA20826, NA19900, HG01377, NA18984, NA18989, NA20322, NA18487, HG01437, HG00553, NA18577, NA20772
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664503
Frequency
Sample Size1151
Observed Gain0
Observed Loss123
Observed Complex0
Frequencyn/a


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