A curated catalogue of human genomic structural variation




Variant Details

Variant: essv20396



Internal ID9618554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86965868..87550005hg38UCSC Ensembl
Innerchr10:88725625..89309762hg19UCSC Ensembl
Innerchr10:88715605..89299742hg18UCSC Ensembl
Innerchr10:88715605..89299742hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38584138
hg19584138
hg18584138
hg17584138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758234
Supporting Variants
SamplesNA10830
Known GenesADIRF, AGAP11, FAM25A, FAM35A, GLUD1, LINC00864, LOC439994, MINPP1, MIR4678, 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)essv20396
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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