A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6887926



Internal ID10282792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:72150561..72150867hg38UCSC Ensembl
Outerchr11:71861605..71861911hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744761, esv2744762
Supporting Variants
SamplesSSM096
Known Genes
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)essv6887926
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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