A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17755



Internal ID9955174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65590162..65750080hg38UCSC Ensembl
Innerchr13:66164294..66324212hg19UCSC Ensembl
Innerchr13:65062295..65222213hg18UCSC Ensembl
Innerchr13:65062295..65222213hg17UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38159919
hg19159919
hg18159919
hg17159919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758330
Supporting Variants
SamplesNA10831
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)essv17755
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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