A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17016



Internal ID9614799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46314456..46836265hg38UCSC Ensembl
Innerchr17:44391822..44913631hg19UCSC Ensembl
Innerchr17:41747597..42268630hg18UCSC Ensembl
Innerchr17:41747597..42268630hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38521810
hg19521810
hg18521034
hg17521034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758457
Supporting Variants
SamplesNA19144
Known GenesARL17A, ARL17B, LRRC37A, LRRC37A2, NSF, NSFP1, WNT3
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)essv17016
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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