A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659026



Internal ID9578445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28534721..28535564hg38UCSC Ensembl
chr7:28574339..28575182hg19UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38844
hg19844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1189e199
Supporting Variantsessv5917052, essv6089289, essv5839266, essv6243011, essv5886942, essv6432084, essv6134875, essv5595184, essv6319866, essv6217623, essv5721602, essv6568572, essv6104249, essv5689924, essv6518309, essv6472032, essv5608389, essv6079408, essv6524464, essv6017367, essv5584417, essv6596370, essv6369710, essv6542943, essv5765020, essv6343329, essv5714610, essv5936775, essv6328648, essv6420046, essv5824229, essv5913070, essv6545099, essv6149881, essv6415626, essv5795743, essv6506101, essv6571722, essv6585850, essv5483577, essv6017489, essv5532999, essv6518799, essv5940011, essv6099985, essv6462987, essv5426144, essv5490490, essv6495258, essv5594033, essv6167444, essv5660487, essv5497674, essv5705185, essv5723821, essv5470058, essv5761569, essv5777854, essv6019735, essv6333661, essv5837679, essv6559407, essv6338274, essv5685824, essv6045507, essv5757110, essv6194510, essv6110036, essv6240518, essv5499908, essv6522780, essv5722341, essv6040374, essv5535990, essv6469808, essv5460061, essv6314992, essv6094305, essv6176823, essv6075541, essv5463291, essv6187589, essv5632281
SamplesHG01441, HG00157, HG00152, HG00734, HG00252, HG01440, HG01072, HG00100, HG00127, HG01173, HG01083, HG00112, HG00731, HG00245, HG00736, HG00261, HG01098, HG01051, HG01365, HG00117, HG01082, HG01488, HG00148, HG00139, HG00106, HG01167, HG01188, HG00111, HG01204, HG01101, HG01134, HG00247, HG00554, HG00115, HG00154, HG01107, HG00158, HG01148, HG00242, HG01140, HG01456, HG00638, HG00259, HG00096, HG01048, HG01061, HG01183, HG00150, HG00258, HG01136, HG00243, HG00133, HG00114, HG00159, HG00124, HG00108, HG01465, HG00233, HG01066, HG00732, HG01069, HG00249, HG00116, HG00103, HG00246, HG01060, HG01383, HG00236, HG01149, HG00120, HG01137, HG01190, HG00262, HG01112, HG01390, HG00123, HG01366, HG01125, HG00119, HG01498, HG00136, HG01067, HG01198
Known GenesCREB5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659026
Frequency
Sample Size1151
Observed Gain0
Observed Loss83
Observed Complex0
Frequencyn/a


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