A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759268



Internal ID9981413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:96588415..96887941hg38UCSC Ensembl
Innerchr4:97509566..97809092hg19UCSC Ensembl
Innerchr4:97728589..98028115hg18UCSC Ensembl
Innerchr4:97866744..98166270hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38299527
hg19299527
hg18299527
hg17299527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757944
SamplesNA18959
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)esv2759268
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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