A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759688



Internal ID9981833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30864034..31038883hg38UCSC Ensembl
Innerchr9:30864032..31038881hg19UCSC Ensembl
Innerchr9:30854032..31028881hg18UCSC Ensembl
Innerchr9:30854032..31028881hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38174850
hg19174850
hg18174850
hg17174850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758187
SamplesNA10856
Known Genes
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)esv2759688
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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