A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6698649



Internal ID9766046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:36756493..36756873hg38UCSC Ensembl
Outerchr11:36778043..36778423hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744350, esv2744353
Supporting Variants
SamplesSSM038
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)essv6698649
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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