A curated catalogue of human genomic structural variation




Variant Details

Variant: esv33415



Internal ID1684537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17532596..17549436hg19UCSC Ensembl
Innerchr11:17489172..17506012hg18UCSC Ensembl
Innerchr11:17489172..17506012hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv100270, essv92533, essv101348
Samples21805, 22233, 22286
Known GenesUSH1C
Method
Analysis
PlatformAgilent-015366 Custom Human 244K CGH Microarray
Comments
Referencede_Smith_et_al_2007
Pubmed ID17666407
Accession Number(s)esv33415
Frequency
Sample Size51
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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