A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6702278



Internal ID9767269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:27635725..27636033hg38UCSC Ensembl
Outerchr11:27657272..27657580hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744294, esv2744293
Supporting Variants
SamplesSSM039
Known GenesBDNF-AS
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)essv6702278
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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