A curated catalogue of human genomic structural variation




Variant Details

Variant: essv23867



Internal ID9622410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87193550..87445609hg38UCSC Ensembl
Innerchr10:88953307..89205366hg19UCSC Ensembl
Innerchr10:88943287..89195346hg18UCSC Ensembl
Innerchr10:88943287..89195346hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38252060
hg19252060
hg18252060
hg17252060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758234
Supporting Variants
SamplesNA12814
Known GenesLINC00864, LOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
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)essv23867
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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