A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2734908



Internal ID9969238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:100991190..101003245hg38UCSC Ensembl
Outerchr7:100634471..100646526hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3812056
hg1912056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1106e201
Supporting Variantsessv6952241, essv6927102, essv6705330, essv6899953, essv6890576, essv6865981, essv6811564, essv6705698, essv6849649, essv6763609, essv6743384, essv6887271, essv6762822, essv6740270, essv6743382, essv6818606, essv6969737, essv6952238, essv6884474, essv6822739, essv6904019, essv6694547, essv6969738, essv6964247, essv6873027, essv6919188, essv6690760, essv6907911, essv6701435, essv6893831, essv6786745, essv6837750, essv6975355, essv6808671, essv6974817, essv6723556, essv6927101, essv6734578, essv6948138, essv6830478, essv6743383, essv6957550, essv6719751, essv6731196, essv6708700, essv6834086, essv6902452, essv6948137, essv6778528, essv6687525, essv6952240, essv6948136, essv6798320, essv6765210, essv6754800, essv6731065, essv6875979, essv6873028, essv6748975, essv6671616, essv6890484, essv6878853, essv6802811, essv6737205, essv6782524, essv6767801, essv6760277, essv6861266, essv6748977, essv6767800, essv6751846, essv6931462, essv6881665, essv6763598, essv6915338, essv6751847, essv6841545, essv6798309, essv6746162, essv6974928, essv6828298, essv6680703, essv6904017, essv6870032, essv6757607, essv6712148, essv6822740, essv6855712, essv6834088, essv6845214, essv6952237, essv6774866
SamplesSSM100, SSM059, SSM036, SSM008, SSM083, SSM027, SSM024, SSM075, SSM045, SSM064, SSM079, SSM087, SSM097, SSM039, SSM013, SSM009, SSM073, SSM093, SSM050, SSM042, SSM088, SSM002, SSM041, SSM057, SSM058, SSM028, SSM092, SSM084, SSM090, SSM047, SSM069, SSM061, SSM029, SSM096, SSM062, SSM026, SSM089, SSM017, SSM019, SSM035, SSM094, SSM003, SSM031, SSM067, SSM044, SSM001, SSM014, SSM086, SSM033, SSM066, SSM006, SSM085, SSM068, SSM081, SSM040, SSM082, SSM007, SSM078, SSM016, SSM053, SSM037, SSM076, SSM010, SSM091, SSM055, SSM095, SSM025, SSM052, SSM098, SSM049, SSM056, SSM063, SSM012
Known GenesMUC12
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2734908
Frequency
Sample Size96
Observed Gain0
Observed Loss73
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer