A curated catalogue of human genomic structural variation




Variant Details

Variant: essv51239



Internal ID11327125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101357737..101363752hg38UCSC Ensembl
Innerchr7:101001018..101007033hg19UCSC Ensembl
Innerchr7:100787738..100793753hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg386016
hg196016
hg186016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv11260
Supporting Variants
SamplesNA11931
Known GenesCOL26A1
MethodOligo aCGH
AnalysisSegment log2 ratios from each sample. This was done running the GADA algorithm (Pique-Regi et al., 2008) using the options "-M 10 -T 10 -a 2.5". Filter non-CNV segments using intensity thresholds. Merge remaining CNV "calls" within each sample. Adjacent calls of the same direction (gain or loss) are merged if both: the distance between calls is less than 10kb, and the distance between calls is less than 10% of the size of the largest of the two calls.
PlatformSanger H. Sapiens 42mCGH Array 5781_53 726K v1
Comments
ReferenceConrad_et_al_2009
Pubmed ID19812545
Accession Number(s)essv51239
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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