A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2001202



Internal ID2427427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:114120076..114120519hg19UCSC Ensembl
Outerchr11:114120029..114120577hg19UCSC Ensembl
Innerchr11:113625286..113625729hg18UCSC Ensembl
Outerchr11:113625239..113625787hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsessv4867243
SamplesNA18507
Known GenesZBTB16
Method
AnalysisRegion identical to calls - DGVa curated
PlatformIllumina GA1 DNA Sequencer
Comments
ReferenceBentley_et_al_2008
Pubmed ID18987734
Accession Number(s)esv2001202
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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