A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6783367



Internal ID9840919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1155269..1155990hg38UCSC Ensembl
Outerchr11:1148880..1149617hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38722
hg19738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743901, esv2743878, esv2743902
Supporting Variants
SamplesSSM068
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)essv6783367
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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