A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759685



Internal ID9981830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29135950..29309830hg38UCSC Ensembl
Innerchr9:29135948..29309828hg19UCSC Ensembl
Innerchr9:29125948..29299828hg18UCSC Ensembl
Innerchr9:29125948..29299828hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38173881
hg19173881
hg18173881
hg17173881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758184
SamplesNA19193
Known GenesLINGO2
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)esv2759685
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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