A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6884957



Internal ID10279767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:7407341..7407701hg38UCSC Ensembl
Outerchr11:7428572..7428932hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744079
Supporting Variants
SamplesSSM095
Known GenesSYT9
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)essv6884957
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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