A curated catalogue of human genomic structural variation




Variant Details

Variant: essv81771



Internal ID11017429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11928997..11934452hg38UCSC Ensembl
Innerchr19:12039812..12045267hg19UCSC Ensembl
Innerchr19:11900812..11906267hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385456
hg195456
hg185456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv16325
Supporting Variants
SamplesNA19114
Known GenesZNF700
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)essv81771
Frequency
Sample Size40
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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