A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757759



Internal ID9979836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166522642..166681748hg38UCSC Ensembl
Innerchr1:166491879..166650985hg19UCSC Ensembl
Innerchr1:164758503..164917609hg18UCSC Ensembl
Innerchr1:163223537..163382643hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38159107
hg19159107
hg18159107
hg17159107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2758975
Supporting Variantsessv4558
SamplesNA18524
Known GenesFMO9P
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)esv2757759
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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