A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757963



Internal ID9980040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161456617..161638558hg38UCSC Ensembl
Innerchr4:162377769..162559710hg19UCSC Ensembl
Innerchr4:162597219..162779160hg18UCSC Ensembl
Innerchr4:162735374..162917315hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38181942
hg19181942
hg18181942
hg17181942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759296
Supporting Variantsessv11928
SamplesNA18502
Known GenesFSTL5
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)esv2757963
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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