A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6891161



Internal ID10285526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:56700448..56740269hg38UCSC Ensembl
Outerchr11:56467924..56507745hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3839822
hg1939822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744543
Supporting Variants
SamplesSSM097
Known GenesOR9G1, OR9G9
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)essv6891161
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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