A curated catalogue of human genomic structural variation




Variant Details

Variant: esv20185



Internal ID11037419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16508255..16693048hg38UCSC Ensembl
Innerchr1:16834750..17019543hg19UCSC Ensembl
Innerchr1:16707337..16892130hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38184794
hg19184794
hg18184794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv29642
Supporting Variantsessv76908, essv59165, essv83476, essv38056, essv62761, essv40328, essv55381, essv41884, essv82022, essv72253
SamplesNA19190, NA12878, NA19114, NA15510, NA19099, NA19257, NA19225, NA19108, NA18505, NA18511
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1P2, NBPF1
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)esv20185
Frequency
Sample Size40
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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