A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660941



Internal ID9927046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128356700..128356850hg38UCSC Ensembl
chr9:131118979..131119129hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5473912, essv5902344, essv5970059, essv5918122, essv5756251, essv5813123, essv6316269, essv6037260, essv5441036, essv6190367, essv5840739, essv5871180, essv5463016, essv5795488, essv5715314, essv5650228, essv5950649, essv6457706, essv6047267, essv5408649, essv6040799, essv6271070, essv5980777, essv5457624, essv5650429, essv5628797, essv5889720, essv5914029, essv6019468, essv6140397, essv6066043, essv5650593, essv6254005, essv5438848, essv6385582, essv5489843, essv5850804, essv6322429, essv6242621, essv5915263, essv6168613, essv5525261, essv6205425, essv6191893, essv5396216, essv5563761, essv6580284, essv5718268, essv5435659, essv5934298, essv6385717, essv5524620, essv6008059, essv5778875, essv5628374, essv5707604, essv6457292, essv5402163, essv6216225, essv5988272, essv5444394, essv6431923, essv5773346, essv6039589, essv6039028, essv5903413, essv5854531, essv5627913, essv6439051, essv6494372, essv6084776, essv6312051, essv6538167, essv6381719, essv5683286, essv5997298, essv5938895, essv6509671, essv5470780, essv5424534, essv6389331, essv5778017, essv6145675, essv6103398, essv6372905, essv5619107, essv5873731, essv5633058, essv6447701, essv6409179, essv6573133, essv5898969, essv5694616, essv6411420, essv6126265, essv5822998, essv5701019, essv6084341, essv6301650, essv5746714, essv5974771, essv6457045, essv6378902, essv5462375, essv5764341, essv6140849
SamplesNA19701, HG00542, NA18621, NA10851, NA18980, NA19704, NA18599, NA19355, NA18530, HG00449, NA20507, HG00654, HG01051, NA19067, HG00693, NA18988, NA12413, NA19076, NA19005, HG00272, NA18489, HG00702, NA18582, NA19088, NA20287, NA19384, NA19130, HG00590, NA12275, NA19651, NA18874, HG01495, NA19719, NA19371, NA18560, NA19235, NA18617, NA19471, HG01440, NA19002, HG00118, NA19189, NA18985, NA19985, NA18867, HG00419, NA19789, HG00543, HG00133, NA18613, NA18538, NA12003, HG00653, NA20314, NA19663, HG00583, NA19081, NA18910, NA18871, NA19776, HG00708, NA19084, HG00690, HG01197, HG00684, NA18532, NA19059, NA19761, NA19009, NA18963, NA19756, HG00463, HG01107, NA18945, NA18576, NA20296, HG00258, NA19729, NA18535, NA19147, NA19331, HG00098, HG01375, HG00237, NA19786, NA19083, HG01108, HG00662, NA18610, NA12347, NA20341, NA19376, HG00513, NA19472, HG00421, HG00656, NA19713, NA20289, NA18873, HG00698, HG00280, NA19004, NA18623, NA19065, NA18549, HG00553
Known GenesSLC27A4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660941
Frequency
Sample Size1151
Observed Gain0
Observed Loss106
Observed Complex0
Frequencyn/a


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