A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665098



Internal ID9931203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37764660..37764988hg38UCSC Ensembl
chr4:37766282..37766610hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6261666, essv5714060, essv6469488, essv6018016, essv5901620, essv5574807, essv6228051, essv5419409, essv6356069, essv5583665, essv5931246, essv5918711, essv5591804, essv5401520, essv5892225, essv6585262, essv6515971, essv6252431, essv5864330, essv5469345, essv5853206, essv5870827, essv6594527, essv5408763, essv6567033, essv6043963, essv6311952, essv6206657, essv5571060, essv6472203, essv6260984, essv6567819, essv5626175, essv6276508, essv5702635, essv5981347, essv6536119, essv5633847, essv5770058, essv6219272, essv6210154, essv6315196, essv5902445, essv5434414, essv6498037, essv6252186, essv5767911, essv5397561, essv6066913, essv6502244, essv5641179, essv6242953, essv5462160, essv6386855, essv6563593, essv6523338, essv6339045, essv5611357, essv6208321, essv6079970, essv6117908, essv5613943, essv6084207, essv5701530, essv6537631, essv5795114, essv5422168, essv6104854, essv5978787, essv5553670, essv5520582, essv6315518, essv5576603, essv6068718, essv5768699, essv5456069, essv6496947, essv5398792, essv5856963, essv6455392, essv6382708, essv6086270, essv5458874, essv5677425, essv6243747, essv5818030, essv6350261, essv6100812, essv5624053, essv5801632, essv6439337, essv5738354, essv5533070, essv5519704, essv5666820, essv6248996, essv6046518, essv6004044, essv5737640, essv6490268, essv5712381, essv5537203, essv5479814, essv6360851, essv6038763, essv6572394, essv6361064, essv5761725, essv6382615, essv5599287, essv5410897, essv5554354, essv6583588, essv6302826, essv6465343, essv5976051, essv5777014, essv5735104, essv6095845, essv6357100, essv5843617, essv6202484, essv6135200, essv6437169, essv6376181, essv5835206
SamplesNA19394, NA18502, HG01060, HG01441, HG00650, NA19058, HG00592, NA12842, NA19703, HG00536, NA19664, NA19466, HG00671, NA19066, NA18565, NA19704, HG01188, NA18599, HG01389, NA20532, HG00318, NA18486, HG00699, NA19355, NA18545, HG00566, NA20332, NA18606, NA19443, NA18870, HG01051, NA18510, NA12399, NA18988, NA19374, NA19660, NA19381, NA19076, NA19382, NA19315, NA18597, NA19678, HG00689, NA18567, NA18618, NA18582, NA20768, NA18571, HG01365, NA19782, NA19904, HG00590, HG01134, NA12275, NA18868, NA19372, NA12044, HG00534, HG00422, HG01440, HG01550, HG00419, NA19789, NA18539, NA19451, NA12748, HG01124, NA19007, NA11831, HG00543, HG01187, NA19670, NA19403, NA19462, HG00475, NA19663, HG00500, HG00275, HG00635, NA19064, NA18907, HG01073, NA19114, HG00531, HG00479, NA12829, HG01197, HG00684, NA19452, HG00463, HG00246, NA19395, NA18858, NA12546, NA19675, HG01204, NA19436, NA19440, NA19390, NA19712, NA18564, NA19749, NA19380, NA19470, HG01137, HG00116, NA18943, HG01108, NA19783, NA19376, NA18631, NA19716, NA19093, NA20289, NA19102, NA19900, NA19430, NA18989, HG01082, HG01125, NA18511, NA18622, HG00581, NA19431, NA18577, NA18620
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665098
Frequency
Sample Size1151
Observed Gain0
Observed Loss126
Observed Complex0
Frequencyn/a


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