A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737297



Internal ID10320933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:91827845..91828302hg38UCSC Ensembl
Outerchr8:92840073..92840530hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6873266, essv6841878, essv6808923, essv6712473, essv6830753, essv6894118, essv6934085, essv6887539, essv6694894, essv6845495, essv6684573, essv6795389, essv6948460, essv6708999, essv6803065, essv6701795, essv6716186, essv6893765, essv6897215, essv6677215, essv6944229, essv6691089, essv6838059, essv6850222, essv6778863, essv6799581, essv6870302, essv6970123, essv6879079, essv6856250, essv6923697, essv6672156, essv6931176, essv6731524, essv6782916, essv6834380, essv6958194, essv6830769, essv6791224, essv6827085
SamplesSSM036, SSM083, SSM071, SSM024, SSM075, SSM087, SSM039, SSM073, SSM093, SSM042, SSM041, SSM023, SSM028, SSM084, SSM090, SSM047, SSM018, SSM096, SSM026, SSM032, SSM003, SSM031, SSM067, SSM086, SSM085, SSM068, SSM081, SSM072, SSM082, SSM020, SSM080, SSM037, SSM010, SSM091, SSM070, SSM034, SSM099, SSM043, SSM098, SSM012
Known Genes
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)esv2737297
Frequency
Sample Size96
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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