A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7123



Internal ID9629000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132412726..132613563hg38UCSC Ensembl
Innerchr10:134226230..134427067hg19UCSC Ensembl
Innerchr10:134076220..134277057hg18UCSC Ensembl
Innerchr10:134076220..134277057hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38200838
hg19200838
hg18200838
hg17200838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758246
Supporting Variants
SamplesNA18537
Known GenesC10orf91, INPP5A, PWWP2B
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)essv7123
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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