A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659146



Internal ID9578565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155560528..155573651hg38UCSC Ensembl
chrX:154790189..154803312hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3813124
hg1913124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6171527, essv6437778, essv5893322, essv5585872, essv6439648, essv6486058, essv5432850, essv5526758, essv6500757, essv5612682, essv6558862, essv6055151, essv5586638, essv5458868, essv5777822, essv5516559, essv6401501, essv5700070, essv6583965, essv5470761, essv5659914, essv5771351, essv5456348, essv6349823, essv5925000, essv6283919, essv6047513, essv5546994, essv5767147, essv5871800, essv6275735, essv5701368, essv6264636, essv6243840, essv5588427, essv5790377, essv5913239, essv5696202, essv5408437, essv5775132, essv6329259, essv5673563, essv5748309, essv6199916, essv6013129, essv6250976, essv6202311, essv6395145, essv5705094, essv5922991, essv5567591, essv6020772, essv6056450, essv5802508, essv5603884, essv5919400, essv6205658, essv5696849, essv5681201, essv6292958, essv5727212, essv6155328, essv6517380, essv6234387, essv6127292, essv6435753, essv5534846, essv5792178, essv6491046, essv6181115, essv5626314, essv6422751, essv6204258, essv5621695, essv5778034, essv6463152, essv6015032, essv6566773, essv5912597, essv6017955, essv6498353, essv5712276, essv5547708, essv5875113, essv6073298, essv6535559, essv5484788, essv6142803, essv6204856, essv6359993, essv5796387, essv6120666, essv6082806, essv5881570, essv6067343, essv6582600, essv5839117, essv5399417, essv5553322, essv6435293, essv6349931, essv6245480, essv5646334, essv6126787, essv6205771, essv6166889, essv5857328, essv5635125, essv5823681
SamplesHG00309, HG01515, NA12718, HG00313, HG01518, HG00252, HG00536, HG00182, HG00344, HG01353, HG01072, HG01519, HG00328, HG00500, HG01173, HG00171, HG00463, HG00657, HG00189, HG00375, HG01174, HG00270, HG01350, HG00139, HG00683, HG00334, HG00404, HG00557, HG01134, NA19682, HG00177, HG00331, NA19780, HG01171, NA18626, HG00479, NA18628, HG00554, HG01521, HG00342, HG00154, HG00242, NA19085, HG00346, HG00179, HG00250, HG01140, HG00583, HG00337, NA19675, NA18623, HG00610, HG01061, HG00231, HG00689, NA12273, HG00330, HG00338, HG00178, HG00125, HG00258, HG01136, HG00174, HG00357, NA20589, HG00237, HG00343, HG00584, HG00306, HG00620, HG01516, HG00185, HG00559, HG00176, HG00560, HG00265, HG00282, HG00249, NA20818, HG00277, HG00513, HG00524, HG00329, HG00525, HG01060, HG00589, HG01149, HG01137, HG00595, NA19078, HG00118, HG00448, NA18602, NA20509, HG00281, HG00285, HG00422, HG00693, HG00566, HG01125, HG00251, HG00275, HG00324, HG00625, HG00690, HG01522, HG00671, HG00702, HG00327
Known GenesTMLHE
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659146
Frequency
Sample Size1151
Observed Gain0
Observed Loss109
Observed Complex0
Frequencyn/a


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