A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757873



Internal ID9979950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61033331..61199884hg38UCSC Ensembl
Innerchr3:61019003..61185558hg19UCSC Ensembl
Innerchr3:60994043..61160598hg18UCSC Ensembl
Innerchr3:60994043..61160598hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38166554
hg19166556
hg18166556
hg17166556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759152
Supporting Variantsessv24815, essv5509, essv24600
SamplesNA11992, NA18632, NA10860
Known GenesFHIT
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)esv2757873
Frequency
Sample Size270
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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