A curated catalogue of human genomic structural variation




Variant Details

Variant: esv22273



Internal ID11039506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44739402..44743078hg38UCSC Ensembl
Innerchr22:45135282..45138958hg19UCSC Ensembl
Innerchr22:43513946..43517622hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383677
hg193677
hg183677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv12992, esv19395, esv17218, esv17848
SamplesNA18861, NA12004, NA19190, NA07045, NA15510, NA19099, NA19225, NA18523, NA18858, NA18909, NA18505
Known GenesPRR5-ARHGAP8
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)esv22273
Frequency
Sample Size40
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer