A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2736750



Internal ID5047482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:22886376..23058657hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6841827, essv6830398, essv6795324, essv6890719, essv6795323, essv6866319, essv6939669, essv6904451, essv6860387, essv6723867, essv6870254, essv6856158, essv6799517, essv6746360, essv6701737, essv6694845, essv6733499, essv6866318, essv6931127, essv6838007, essv6701735, essv6749203, essv6731477, essv6803024, essv6856157, essv6890718, essv6876189, essv6919503, essv6873224, essv6677157, essv6850132, essv6944161, essv6894073, essv6915593, essv6944163, essv6705630, essv6830729, essv6838008, essv6958093, essv6884660, essv6841826, essv6672056, essv6911947, essv6850133, essv6791179, essv6958092, essv6805899, essv6923648, essv6822981, essv6808875, essv6727713, essv6683066, essv6900152, essv6765392, essv6915592, essv6944160, essv6701736, essv6727708, essv6814873, essv6873223, essv6811757, essv6830730, essv6795325, essv6677158, essv6970065, essv6768014, essv6762984, essv6723868, essv6879039, essv6755025, essv6964701, essv6800643, essv6712423, essv6782853, essv6893277, essv6904317, essv6787071, essv6927370, essv6900151, essv6716141, essv6720059, essv6791178, essv6771426, essv6733510, essv6727712, essv6672054, essv6966217, essv6727711, essv6845451, essv6708956, essv6822982, essv6708955, essv6737419
SamplesSSM010, SSM065, SSM022, SSM007, SSM027, SSM092, SSM013, SSM086, SSM055, SSM091, SSM084, SSM042, SSM040, SSM043, SSM089, SSM090, SSM064, SSM031, SSM072, SSM020, SSM071, SSM016, SSM032, SSM039, SSM045, SSM083, SSM050, SSM097, SSM041, SSM077, SSM062, SSM005, SSM012, SSM093, SSM100, SSM056, SSM085, SSM017, SSM009, SSM011, SSM028, SSM095, SSM047, SSM073, SSM069, SSM002, SSM037, SSM063, SSM087, SSM046, SSM019, SSM023, SSM079, SSM068, SSM044, SSM074, SSM004, SSM075, SSM015, SSM026, SSM098, SSM018, SSM076, SSM058, SSM081, SSM070
Known GenesLOC286059, TNFRSF10A, TNFRSF10B, TNFRSF10C, TNFRSF10D
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2736750
Frequency
Sample Size96
Observed Gain0
Observed Loss66
Observed Complex0
Frequencyn/a


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