A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758177



Internal ID9633636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5297921..5454512hg38UCSC Ensembl
Innerchr9:5297921..5454512hg19UCSC Ensembl
Innerchr9:5287921..5444512hg18UCSC Ensembl
Innerchr9:5287921..5444512hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38156592
hg19156592
hg18156592
hg17156592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759660
Supporting Variantsessv24412
SamplesNA12707
Known GenesCD274, PLGRKT, RLN1, RLN2
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)esv2758177
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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