A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759191



Internal ID9981336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154540480..154840934hg38UCSC Ensembl
Innerchr3:154258269..154558723hg19UCSC Ensembl
Innerchr3:155740963..156041417hg18UCSC Ensembl
Innerchr3:155740971..156041425hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38300455
hg19300455
hg18300455
hg17300455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757899
SamplesNA19201, NA19202
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)esv2759191
Frequency
Sample Size270
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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