A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13593



Internal ID9610995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143712969..143951396hg38UCSC Ensembl
Innerchr4:144634122..144872549hg19UCSC Ensembl
Innerchr4:144853572..145091999hg18UCSC Ensembl
Innerchr4:144991727..145230154hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38238428
hg19238428
hg18238428
hg17238428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757960
Supporting Variants
SamplesNA19127
Known GenesGYPE
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)essv13593
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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