A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759673



Internal ID9981818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16641968..16809205hg38UCSC Ensembl
Innerchr9:16641966..16809203hg19UCSC Ensembl
Innerchr9:16631966..16799203hg18UCSC Ensembl
Innerchr9:16631966..16799203hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38167238
hg19167238
hg18167238
hg17167238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758627
SamplesNA12006
Known GenesBNC2
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)esv2759673
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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