A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737993



Internal ID10321629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:143316395..143316595hg38UCSC Ensembl
Outerchr8:144398565..144398765hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6856345, essv6870347, essv6958317, essv6861732, essv6866463, essv6672269, essv6850334, essv6819052
SamplesSSM087, SSM088, SSM090, SSM026, SSM089, SSM031, SSM086, SSM078
Known GenesTOP1MT
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)esv2737993
Frequency
Sample Size96
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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