A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15256



Internal ID9612843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22282297..22591105hg38UCSC Ensembl
Innerchr17:21808903..22090432hg19UCSC Ensembl
Innerchr17:21733030..22014559hg18UCSC Ensembl
Innerchr17:21733030..22014559hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38308809
hg19281530
hg18281530
hg17281530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758446
Supporting Variants
SamplesNA19094
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv15256
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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