A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16873



Internal ID9614639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37864474..38062733hg38UCSC Ensembl
Innerchr3:37905965..38104224hg19UCSC Ensembl
Innerchr3:37880969..38079228hg18UCSC Ensembl
Innerchr3:37880969..38079228hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38198260
hg19198260
hg18198260
hg17198260
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757866
Supporting Variants
SamplesNA19205
Known GenesCTDSPL, DLEC1, MIR26A1, PLCD1, VILL
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)essv16873
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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