A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2743591



Internal ID9977875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131952794..131953047hg38UCSC Ensembl
Outerchr10:133766298..133766551hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6731899, essv6672805, essv6791623, essv6783335
SamplesSSM031, SSM047, SSM068, SSM070
Known GenesPPP2R2D
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)esv2743591
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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