A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666173



Internal ID9932278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120516931..120517657hg38UCSC Ensembl
chr11:120387640..120388366hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5506486, essv6550453, essv6507609, essv6273906, essv5571190, essv5769555, essv5454124, essv6524505, essv6557394, essv5742500, essv6478293, essv6003616, essv5711986, essv6154047, essv5644372, essv6059546, essv5840491, essv6274373, essv5523699, essv5661060, essv6413885, essv6323291, essv6397719, essv6330306, essv6556071, essv6384677, essv5447807, essv6547425, essv5899359, essv5705640, essv6318874, essv6123522, essv6268975, essv5982833, essv6523271, essv6002831, essv6093559, essv6155428, essv6511371, essv6121969, essv6311354, essv5409739, essv6396074, essv6219186, essv5962790, essv5772815, essv6366698, essv5903574, essv5593207, essv5841514, essv6441774, essv6090724, essv5525612, essv6246736, essv6445030, essv5587891, essv6593138, essv5765284, essv5761291, essv5788499, essv5478355, essv5408292, essv5898645, essv6508333, essv6352010, essv5976087, essv5953907, essv5938708, essv6069956, essv6262306, essv6055366, essv6521837, essv5743084, essv5854199, essv6213239, essv6596028, essv5948088, essv5567669, essv5781767, essv6285088, essv6255218, essv5881181, essv5424641, essv6185878, essv5871849, essv6532733, essv6558469, essv5593657, essv5978505, essv5473450, essv6214229, essv5789951, essv5565659, essv6492937, essv6057749, essv6287326, essv5474738
SamplesNA19701, HG00650, NA12842, HG00231, NA18924, NA20783, NA12414, NA12843, HG00315, NA20512, NA18486, NA12751, NA19355, NA19393, NA20808, NA19098, NA18602, NA12813, NA18944, NA18519, HG00272, NA18489, NA20798, NA19723, NA18982, NA18960, HG01067, NA19383, HG01519, NA19917, HG01072, NA18560, NA19385, NA19159, NA19239, NA19445, NA18867, NA19451, NA12748, HG00260, HG00188, NA18951, HG01187, NA19707, NA19347, NA19152, NA20810, NA19455, NA18516, NA18910, NA18981, HG00708, NA18907, NA19114, NA18856, NA19453, NA18912, HG00157, HG01334, NA18523, NA19318, NA19160, HG00126, NA19625, NA19675, NA18953, NA19401, NA18909, NA18517, NA19434, NA18950, NA19240, NA20530, NA20527, NA19679, HG01108, HG00256, NA12763, HG00339, NA19376, NA19248, NA19468, HG01055, HG00310, NA20786, NA19102, NA20807, HG00343, NA20528, NA18984, NA07056, NA19129, NA18488, NA18623, NA20754, HG00553, NA18965
Known GenesGRIK4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666173
Frequency
Sample Size1151
Observed Gain0
Observed Loss97
Observed Complex0
Frequencyn/a


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