A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6845733



Internal ID9897955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:94680649..94902474hg38UCSC Ensembl
Outerchr10:96440406..96662231hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38221826
hg19221826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2739707
Supporting Variants
SamplesSSM085
Known GenesCYP2C18, CYP2C19
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)essv6845733
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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