A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10073



Internal ID9973123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120960420..121142359hg38UCSC Ensembl
Innerchr10:122719933..122901873hg19UCSC Ensembl
Innerchr10:122709923..122891863hg18UCSC Ensembl
Innerchr10:122709923..122891863hg17UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38181940
hg19181941
hg18181941
hg17181941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758241
Supporting Variants
SamplesNA19099
Known GenesMIR5694
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)essv10073
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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