A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759244



Internal ID9981389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:31613503..31800324hg38UCSC Ensembl
Innerchr4:31615125..31801946hg19UCSC Ensembl
Innerchr4:31224223..31411039hg18UCSC Ensembl
Innerchr4:31291394..31478210hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38186822
hg19186822
hg18186817
hg17186817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2757929
SamplesNA18855
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)esv2759244
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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