A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6882202



Internal ID9930778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:27635727..27636032hg38UCSC Ensembl
Outerchr11:27657274..27657579hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744294, esv2744293
Supporting Variants
SamplesSSM094
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)essv6882202
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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