A curated catalogue of human genomic structural variation




Variant Details

Variant: essv49251



Internal ID10977383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:629749..773482hg38UCSC Ensembl
Innerchr1:565129..708862hg19UCSC Ensembl
Innerchr1:554992..698725hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38143734
hg19143734
hg18143734
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv20880
Supporting Variants
SamplesNA07037
Known GenesLOC100133331, LOC100288069, MIR6723, OR4F16, OR4F29, OR4F3
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)essv49251
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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