A curated catalogue of human genomic structural variation




Variant Details

Variant: esv26756



Internal ID11043989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:4772529..4855231hg38UCSC Ensembl
Innerchr16:4822530..4905232hg19UCSC Ensembl
Innerchr16:4762531..4845233hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3882703
hg1982703
hg1882703
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv10759, esv13855, esv21156, esv12201
SamplesNA07037, NA18511, NA19190, NA07045
Known GenesGLYR1, ROGDI, SEPT12, SMIM22, UBN1
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)esv26756
Frequency
Sample Size40
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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