A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670257



Internal ID9589676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151410355..151413661hg38UCSC Ensembl
Outerchr5:151409884..151414331hg38UCSC Ensembl
Innerchr5:150789916..150793222hg19UCSC Ensembl
Outerchr5:150789445..150793892hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg384448
hg194448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5555148, essv6343442, essv6054239, essv5767210, essv5723370, essv5750755, essv6297194, essv6307929, essv5956480, essv5970127, essv6305204, essv6193902, essv6377042, essv6185129, essv5959095, essv5618952, essv6337010, essv6346108, essv6015461, essv6413426, essv5961005, essv6088693, essv6305882, essv5747371, essv6085760, essv6097772, essv5934020, essv6235692, essv6410661, essv6463237, essv6169649, essv6596357, essv5578316, essv6053317, essv6551861, essv5763199, essv5712488, essv6228831, essv6477855, essv6535352, essv5958095, essv6173784, essv6574994, essv5840763, essv6333332, essv6497059, essv5527355, essv5877358, essv6419067, essv5656513, essv5729685, essv5678135, essv6069359, essv6436358, essv5583356, essv5718940, essv5886067, essv6359292, essv6328253, essv6350903, essv6501651, essv5655997, essv6340994, essv5457921, essv5590751, essv5732390, essv6029350, essv5614749, essv6047885, essv5616228, essv5608253, essv5508298, essv5600943, essv5823446, essv5594757, essv5761616, essv5514841, essv6437965, essv6238695, essv5968291, essv6174293, essv5507413, essv6027484, essv5486759, essv5729865, essv5937595, essv5761016, essv5720172, essv6200420, essv6451889, essv6289434, essv5428375, essv5849159, essv6270064, essv5448883, essv5916982, essv5491788, essv6154309, essv5838221, essv6202021, essv6446981, essv5420350, essv5783488, essv6072853, essv6466334, essv5815201, essv5628974, essv5761598, essv6256463, essv6100723, essv6110471, essv6092151, essv5532023, essv6245904, essv5560564, essv5518880, essv5617315, essv5521472, essv5905333, essv5929565, essv6281418, essv5480167, essv6369897, essv6500192, essv6228334, essv6244130, essv5689718, essv5874694, essv5889125, essv5785968, essv6043472, essv5938152, essv5663398, essv5982626, essv6113187
SamplesHG00542, HG00442, NA19058, NA19055, HG00608, NA18621, NA11829, HG00671, NA19066, NA18592, HG00559, HG00524, NA18565, NA18561, NA18599, NA12751, NA19057, NA18530, NA12058, NA18959, NA18526, NA12400, NA12399, NA19067, NA12341, NA12813, NA18967, NA18563, NA18940, HG00501, HG00702, NA18982, NA18547, HG00634, NA18942, NA11918, NA18582, NA19088, NA19054, NA18964, HG00537, NA19079, NA18949, HG00590, HG00512, NA12282, NA18977, NA11932, NA18560, HG00422, NA19087, HG00427, NA18985, NA18973, HG00530, HG00419, NA19007, NA18614, NA10847, HG00543, NA18951, NA18544, HG00629, HG00443, NA19056, HG00596, HG00557, HG00701, HG00475, HG00436, HG00583, NA18637, NA18572, HG00619, HG00708, NA18548, NA18566, NA18573, HG00651, NA19000, HG00690, HG00479, NA18532, HG00613, NA19059, NA18555, NA18963, HG00704, NA18536, NA18570, NA18593, NA12546, NA18541, NA19012, NA18576, NA18535, NA18564, NA18628, NA19072, NA18941, NA07051, NA19010, HG00473, HG00662, HG00418, NA12347, NA06986, HG00620, NA19078, HG00614, HG00478, NA18971, NA18631, HG00421, NA18987, HG00656, NA18636, NA12830, NA18609, HG00698, NA11843, NA18552, NA18983, NA18984, NA07056, NA18989, NA11892, NA12890, NA18623, NA19063, NA19065, NA19074, NA18622, NA12776, HG00593
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670257
Frequency
Sample Size1151
Observed Gain0
Observed Loss135
Observed Complex0
Frequencyn/a


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