A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759167



Internal ID9981312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106431983..106616496hg38UCSC Ensembl
Innerchr3:106150830..106335343hg19UCSC Ensembl
Innerchr3:107633520..107818033hg18UCSC Ensembl
Innerchr3:107633520..107818033hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38184514
hg19184514
hg18184514
hg17184514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757884
SamplesNA10856
Known Genes
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)esv2759167
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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