A curated catalogue of human genomic structural variation




Variant Details

Variant: esv26238



Internal ID11043471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79066222..79071664hg38UCSC Ensembl
Innerchr10:80825979..80831421hg19UCSC Ensembl
Innerchr10:80495985..80501427hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385443
hg195443
hg185443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv12224
SamplesNA07037, NA11995, NA07045, NA12156, NA12878
Known GenesZMIZ1, ZMIZ1-AS1
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)esv26238
Frequency
Sample Size40
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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