A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659348



Internal ID9578767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29453314..29454037hg38UCSC Ensembl
chr10:29742243..29742966hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5702213, essv6112625, essv5857118, essv6094356, essv5397895, essv5822214, essv6413992, essv6536225, essv5921090, essv6432051, essv5667946, essv6139899, essv6179558, essv5413352, essv6232602, essv6467039, essv6135449, essv6385068, essv5857237, essv6337335, essv5824470, essv5951961, essv5771656, essv6030081, essv5784990, essv6465937, essv5396381, essv5536039, essv6467611, essv5423590, essv5464519, essv5555744, essv5716533, essv6169227, essv6298877, essv6412219, essv6580404, essv6070315, essv5576984, essv5771197, essv6261319, essv5491660, essv5948154, essv6581873, essv5636315, essv5778935, essv5952254, essv5633356, essv6003207, essv5738752, essv6422768, essv6385741, essv5813746, essv5556700, essv6022437, essv5716220, essv6240539, essv6430216, essv6369720, essv5796881, essv5597299, essv6480810, essv5662638, essv5645611, essv6173890, essv5837191, essv6202467, essv6053058, essv5515563, essv6247008, essv5495626, essv6172388, essv5901213, essv6484179, essv5440278, essv6456738, essv5483741, essv5800520, essv6402223, essv6062879, essv5715905, essv5678772, essv6030485, essv6508628, essv5753105, essv6297662, essv6493421, essv5992717, essv6108850, essv5693649, essv5927110, essv6467345, essv6378535, essv5641163, essv6432762, essv6456215, essv6361319
SamplesHG00309, NA12154, NA12043, HG00152, HG00252, NA07347, NA12750, NA20527, HG00344, NA12286, NA20506, HG00328, NA11920, HG01083, HG00112, HG00186, NA12347, HG01197, NA12813, HG00189, NA12828, NA19782, HG00139, HG00106, NA12058, HG01461, NA19678, NA19701, HG00146, HG00319, HG00253, NA20803, HG00156, NA19776, HG00266, NA19762, HG00339, NA20585, NA12763, NA12843, NA19675, HG00180, HG01061, HG01047, NA20807, HG00141, NA12273, HG00330, HG01136, NA11894, NA12400, HG00264, NA19679, HG00276, HG00284, NA12830, HG00343, NA12144, HG00306, HG00267, HG00108, NA19172, NA12892, HG00268, HG00325, NA06986, NA19238, NA20334, HG00147, NA19731, HG00273, HG00249, NA11892, NA20582, NA20766, NA19711, HG00120, HG00151, NA12891, NA10851, NA19138, HG01334, NA12749, NA20276, NA20799, HG00138, HG00118, NA12878, NA20507, NA11992, HG00281, NA12546, NA20792, NA19240, HG00275, NA12717, HG00361
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659348
Frequency
Sample Size1151
Observed Gain0
Observed Loss97
Observed Complex0
Frequencyn/a


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