A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2732753

Internal ID9967074
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:136276430..136277868hg38UCSC Ensembl
Outerchr6:136597568..136599006hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6680483, essv6814416, essv6875814, essv6805525, essv6818358, essv6826508, essv6855998, essv6887090, essv6926899, essv6782306, essv6872848, essv6671255, essv6729664, essv6808518, essv6727210, essv6701184, essv6723318, essv6794757, essv6690564, essv6952001, essv6765089, essv6899784, essv6893626, essv6743248, essv6826787, essv6811406, essv6694257, essv6704465, essv6730970, essv6896845, essv6884314, essv6929540, essv6837526, essv6969465, essv6796443, essv6684080, essv6869848, essv6974952, essv6711929, essv6830268, essv6774671, essv6943539, essv6939116, essv6746022, essv6841349, essv6915145, essv6822530, essv6778294, essv6790603, essv6878696, essv6734434, essv6748829, essv6923161, essv6760119, essv6897264, essv6881505, essv6697995, essv6962117, essv6705125, essv6667625, essv6907690, essv6754634, essv6888722, essv6934832, essv6903806, essv6679610, essv6963883, essv6767620, essv6676673, essv6845040, essv6761775, essv6762705, essv6798963, essv6715626, essv6911440, essv6708524, essv6802648, essv6855373, essv6930542, essv6849284, essv6757476, essv6947900, essv6865708, essv6918926, essv6957171, essv6786492, essv6719536, essv6737035, essv6770914, essv6860988, essv6740063, essv6833864
SamplesSSM010, SSM065, SSM022, SSM007, SSM027, SSM092, SSM013, SSM053, SSM082, SSM086, SSM006, SSM036, SSM055, SSM091, SSM033, SSM084, SSM061, SSM099, SSM042, SSM040, SSM078, SSM043, SSM088, SSM089, SSM090, SSM064, SSM031, SSM025, SSM072, SSM020, SSM071, SSM016, SSM032, SSM039, SSM024, SSM045, SSM067, SSM094, SSM083, SSM050, SSM041, SSM077, SSM062, SSM005, SSM012, SSM093, SSM100, SSM056, SSM085, SSM017, SSM009, SSM011, SSM066, SSM028, SSM029, SSM003, SSM095, SSM030, SSM047, SSM073, SSM069, SSM021, SSM002, SSM037, SSM034, SSM063, SSM087, SSM038, SSM046, SSM019, SSM096, SSM023, SSM079, SSM052, SSM068, SSM044, SSM074, SSM004, SSM075, SSM015, SSM026, SSM014, SSM049, SSM008, SSM098, SSM018, SSM076, SSM058, SSM059, SSM081, SSM070, SSM080
Known GenesBCLAF1
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Pubmed ID23290073
Accession Number(s)esv2732753
Sample Size96
Observed Gain0
Observed Loss92
Observed Complex0

Hosted by The Centre for Applied Genomics
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