A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17768



Internal ID9615633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105047009..105483089hg38UCSC Ensembl
Innerchr14:105513346..105949426hg19UCSC Ensembl
Innerchr14:104584391..105020471hg18UCSC Ensembl
Innerchr14:104584391..105020471hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38436081
hg19436081
hg18436081
hg17436081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758369
Supporting Variants
SamplesNA10831
Known GenesBRF1, BTBD6, CRIP2, GPR132, JAG2, MIR6765, MTA1, NUDT14, PACS2, TEX22
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)essv17768
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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