A curated catalogue of human genomic structural variation




Variant Details

Variant: essv18206



Internal ID9958020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38698859..38861804hg38UCSC Ensembl
Innerchr10:38991990..39154935hg19UCSC Ensembl
Innerchr10:39031996..39194941hg18UCSC Ensembl
Innerchr10:39031996..39194941hg17UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38162946
hg19162946
hg18162946
hg17162946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758214
Supporting Variants
SamplesNA12057
Known Genes
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)essv18206
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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