A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757886



Internal ID9979963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116423283..116588695hg38UCSC Ensembl
Innerchr3:116142130..116307542hg19UCSC Ensembl
Innerchr3:117624820..117790232hg18UCSC Ensembl
Innerchr3:117624820..117790232hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38165413
hg19165413
hg18165413
hg17165413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759171
Supporting Variantsessv6324
SamplesNA18609
Known GenesLSAMP
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)esv2757886
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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