A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6864176



Internal ID9663310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12131019..12131319hg38UCSC Ensembl
Outerchr11:12152566..12152866hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744115
Supporting Variants
SamplesSSM011
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)essv6864176
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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