A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6864097



Internal ID10010012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5763344..5788050hg38UCSC Ensembl
Outerchr11:5784574..5809280hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824707
hg1924707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744067
Supporting Variants
SamplesSSM011
Known GenesOR52N1, OR52N5
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)essv6864097
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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