A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658503



Internal ID9924608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487039..32540745hg38UCSC Ensembl
Outerchr6:32486468..32541115hg38UCSC Ensembl
Innerchr6:32454816..32508522hg19UCSC Ensembl
Outerchr6:32454245..32508892hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3854648
hg1954648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1101e199
Supporting Variantsessv5742216, essv6395436, essv6325141, essv6254319, essv6453006, essv6139105, essv5822491, essv6030511, essv6491929, essv5904049, essv6102916, essv5671211, essv5526829, essv5900108, essv6577313, essv5750098, essv6136232, essv5770322, essv5875587, essv6244960, essv6337912, essv6487667, essv5907559, essv5970939, essv5873961, essv6485394, essv6064907, essv5659917, essv6163152, essv5634310, essv6473515, essv6155284, essv6423115, essv6147045, essv6201978, essv6276544, essv5793096, essv6130276, essv5767603, essv5487484, essv5564815, essv6349883, essv6064689, essv5526828, essv6320873, essv6425425, essv5847773, essv6573759, essv5876655, essv6458006, essv6429625, essv5559127, essv6582118, essv5463813, essv6330045, essv6065749, essv6302108, essv6297229, essv6399270, essv5454431, essv5404974, essv6128526, essv5637706, essv5904820, essv6557600, essv5948052, essv5437683, essv6081384, essv5797664, essv5840342, essv5509810, essv5571094, essv6232871, essv5879608, essv6569406, essv6355205, essv6457431, essv6465031, essv6203395, essv5992551, essv6544875, essv6508535, essv5668532, essv6589009, essv5653578, essv6548130, essv5501450, essv5397706, essv6516173, essv5825693, essv5939383, essv6369016, essv6537811, essv6127791, essv5967451, essv5497199, essv5464290, essv5878957, essv6355243, essv6439172
SamplesHG01060, HG01441, HG01173, HG01098, HG01356, HG01462, HG01359, HG01052, HG01079, HG01188, HG01389, HG01374, HG01066, HG00640, HG01465, HG01456, HG00737, HG01461, HG01051, HG01140, HG01250, HG00641, HG01350, HG01366, HG01070, HG01351, HG01167, HG01168, HG01492, HG00736, HG01354, HG01083, HG01365, HG01455, HG01069, HG01080, HG01067, HG01170, HG01495, HG01072, HG01176, HG01440, HG01198, HG00637, HG01048, HG01550, HG01124, HG01353, HG01183, HG01136, HG00731, HG01360, HG01187, HG01171, HG01384, HG00732, HG01095, HG01498, HG01149, HG00740, HG01047, HG01102, HG01073, HG01197, HG01383, HG01182, HG01101, HG01497, HG01107, HG01204, HG01075, HG01148, HG01190, HG01551, HG01253, HG00734, HG00638, HG01357, HG01174, HG01375, HG01494, HG01113, HG01137, HG01108, HG01489, HG01342, HG01491, HG01254, HG01055, HG01251, HG01377, HG01378, HG01082, HG01125, HG01112, HG01097, HG00554, HG01191, HG01061, HG00553
Known GenesHLA-DRB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658503
Frequency
Sample Size1151
Observed Gain0
Observed Loss100
Observed Complex0
Frequencyn/a


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