A curated catalogue of human genomic structural variation




Variant Details

Variant: esv28667



Internal ID108159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89398696..89400546hg19UCSC Ensembl
Innerchr15:87199700..87201550hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsesv14263
SamplesNA18909, NA12878
Known GenesACAN
Method
AnalysisAt the top level of the hierarchy, all contiguous bases overlapping at least 1bp of a CNV call are merged into a “CNV region” (CNVR).
PlatformSanger H. Sapiens NimbleGen 42M CGH Array
Comments
ReferenceConrad et al 2009
Pubmed ID19812545
Accession Number(s)esv28667
Frequency
Sample Size451
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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