A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17709



Internal ID9615568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75660801..76010691hg38UCSC Ensembl
Innerchr10:77420559..77770449hg19UCSC Ensembl
Innerchr10:77090565..77440455hg18UCSC Ensembl
Innerchr10:77090565..77440455hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38349891
hg19349891
hg18349891
hg17349891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758230, esv2758229
Supporting Variants
SamplesNA12872
Known GenesC10orf11
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)essv17709
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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