A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6866913



Internal ID9917017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12131028..12131301hg38UCSC Ensembl
Outerchr11:12152575..12152848hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744115
Supporting Variants
SamplesSSM089
Known GenesMICAL2
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)essv6866913
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer