A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6695352



Internal ID10108770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1804067..1804236hg38UCSC Ensembl
Outerchr11:1825297..1825466hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743966, esv2743965
Supporting Variants
SamplesSSM037
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)essv6695352
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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