A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737224



Internal ID10320860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:81333910..81334749hg38UCSC Ensembl
Outerchr8:82246145..82246984hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6904364, essv6694889, essv6733865, essv6740546, essv6866378, essv6672140, essv6856237, essv6915636, essv6958182, essv6677206, essv6818974, essv6701788, essv6734807, essv6823033, essv6964785, essv6884699, essv6887535, essv6830709, essv6897212, essv6737452, essv6966595, essv6752119
SamplesSSM027, SSM079, SSM087, SSM039, SSM013, SSM050, SSM057, SSM096, SSM026, SSM089, SSM032, SSM031, SSM007, SSM078, SSM016, SSM037, SSM010, SSM095, SSM004, SSM099, SSM052, SSM049
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)esv2737224
Frequency
Sample Size96
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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