A curated catalogue of human genomic structural variation




Variant Details

Variant: essv24600



Internal ID9957099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60796210..61055456hg38UCSC Ensembl
Innerchr3:60781943..61041128hg19UCSC Ensembl
Innerchr3:60756983..61016168hg18UCSC Ensembl
Innerchr3:60756983..61016168hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38259247
hg19259186
hg18259186
hg17259186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757872, esv2757873
Supporting Variants
SamplesNA11992
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)essv24600
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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