A curated catalogue of human genomic structural variation




Variant Details

Variant: essv69311



Internal ID10985661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45496173..45628388hg38UCSC Ensembl
Innerchr17:43573539..43705754hg19UCSC Ensembl
Innerchr17:40929322..41061537hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38132216
hg19132216
hg18132216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv18131
Supporting Variants
SamplesNA12044
Known GenesCRHR1, LOC644172, LRRC37A4P, MGC57346
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)essv69311
Frequency
Sample Size40
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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