A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6866313



Internal ID9916477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:18597122..18598424hg38UCSC Ensembl
Outerchr8:18454632..18455934hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381303
hg191303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2736701
Supporting Variants
SamplesSSM089
Known GenesPSD3
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)essv6866313
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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