A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2736752

Internal ID9971084
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:23072937..23106406hg38UCSC Ensembl
Outerchr8:22930450..22963919hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6830398, essv6841827, essv6795324, essv6890719, essv6904451, essv6870254, essv6733499, essv6931127, essv6749203, essv6731477, essv6856157, essv6876189, essv6919503, essv6944161, essv6705630, essv6838008, essv6672056, essv6911947, essv6850133, essv6958092, essv6805899, essv6923648, essv6808875, essv6765392, essv6701736, essv6915592, essv6727708, essv6873223, essv6830730, essv6677158, essv6768014, essv6723868, essv6879039, essv6755025, essv6800643, essv6712423, essv6893277, essv6927370, essv6900151, essv6720059, essv6791178, essv6966217, essv6845451, essv6708956, essv6822982, essv6737419
SamplesSSM010, SSM007, SSM092, SSM086, SSM091, SSM084, SSM042, SSM040, SSM090, SSM064, SSM031, SSM020, SSM071, SSM016, SSM032, SSM039, SSM045, SSM083, SSM050, SSM097, SSM041, SSM012, SSM093, SSM100, SSM056, SSM085, SSM017, SSM009, SSM047, SSM002, SSM063, SSM087, SSM046, SSM019, SSM023, SSM079, SSM044, SSM074, SSM004, SSM075, SSM015, SSM026, SSM018, SSM058, SSM081, SSM070
Known GenesLOC254896, LOC286059, TNFRSF10C
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Pubmed ID23290073
Accession Number(s)esv2736752
Sample Size96
Observed Gain0
Observed Loss46
Observed Complex0

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