A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6914989



Internal ID9679379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:3155450..3178864hg38UCSC Ensembl
Outerchr6:3155684..3179098hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3823415
hg1923415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731488
Supporting Variants
SamplesSSM016
Known GenesTUBB2A
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)essv6914989
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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