A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760062



Internal ID9982207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100940885..101120697hg38UCSC Ensembl
Innerchr15:101481090..101660902hg19UCSC Ensembl
Innerchr15:99298613..99478425hg18UCSC Ensembl
Innerchr15:99298613..99478425hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38179813
hg19179813
hg18179813
hg17179813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758401
SamplesNA12815
Known GenesLRRK1
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)esv2760062
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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