A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6940120



Internal ID9700981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1148124..1148730hg38UCSC Ensembl
Outerchr11:1142032..1142638hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743899, esv2743878, esv2743900
Supporting Variants
SamplesSSM022
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)essv6940120
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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