A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2734928

Internal ID9969258
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29423202..29423794hg38UCSC Ensembl
Outerchr10:29712131..29712723hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6870490, essv6806135, essv6904610, essv6944546, essv6923989, essv6720371, essv6879259, essv6931486, essv6894378, essv6775411, essv6695197, essv6688027, essv6787421, essv6965241, essv6970437, essv6856681, essv6771758, essv6927660, essv6887758, essv6734969, essv6740785, essv6876420, essv6952890, essv6958712, essv6791516, essv6685109, essv6861978, essv6873445, essv6724184, essv6827370, essv6896220, essv6768251, essv6709229, essv6832565, essv6716452, essv6908531, essv6691325, essv6783211, essv6948731, essv6803221, essv6743784, essv6884870, essv6712720, essv6749437, essv6698526, essv6799876, essv6906385, essv6919819, essv6809129, essv6976542, essv6765579, essv6702097, essv6834603, essv6823314, essv6681285, essv6850661, essv6735898, essv6779139, essv6731785, essv6831003, essv6845696, essv6897406
SamplesSSM010, SSM065, SSM007, SSM027, SSM092, SSM013, SSM053, SSM082, SSM086, SSM036, SSM091, SSM033, SSM099, SSM042, SSM043, SSM088, SSM090, SSM064, SSM035, SSM025, SSM072, SSM020, SSM039, SSM024, SSM045, SSM067, SSM041, SSM005, SSM012, SSM093, SSM056, SSM085, SSM017, SSM009, SSM066, SSM028, SSM029, SSM095, SSM047, SSM069, SSM002, SSM037, SSM063, SSM087, SSM038, SSM019, SSM096, SSM023, SSM079, SSM052, SSM068, SSM044, SSM074, SSM075, SSM026, SSM014, SSM049, SSM098, SSM018, SSM081, SSM070, SSM080
Known Genes
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Pubmed ID23290073
Accession Number(s)esv2734928
Sample Size96
Observed Gain0
Observed Loss62
Observed Complex0

Hosted by The Centre for Applied Genomics
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