A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758626



Internal ID9634085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6576991..6838660hg38UCSC Ensembl
Innerchr9:6576991..6838660hg19UCSC Ensembl
Innerchr9:6566991..6828660hg18UCSC Ensembl
Innerchr9:6566991..6828660hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38261670
hg19261670
hg18261670
hg17261670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759661
Supporting Variantsessv18172
SamplesNA12057
Known GenesGLDC, KDM4C
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)esv2758626
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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