A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758196



Internal ID9980273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:106388349..106593797hg38UCSC Ensembl
Innerchr9:109150630..109356078hg19UCSC Ensembl
Innerchr9:108190451..108395899hg18UCSC Ensembl
Innerchr9:106230185..106435633hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38205449
hg19205449
hg18205449
hg17205449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759708
Supporting Variantsessv23014
SamplesNA12812
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)esv2758196
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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