A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6852594



Internal ID10250817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:8206987..8207142hg38UCSC Ensembl
Outerchr20:8187634..8187789hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2722153, esv2722154
Supporting Variants
SamplesSSM086
Known GenesPLCB1
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)essv6852594
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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