A curated catalogue of human genomic structural variation




Variant Details

Variant: essv19612



Internal ID9617683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32133694..32529598hg38UCSC Ensembl
Innerchr15:32425895..32821799hg19UCSC Ensembl
Innerchr15:30213187..30609091hg18UCSC Ensembl
Innerchr15:30213187..30609091hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38395905
hg19395905
hg18395905
hg17395905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758375
Supporting Variants
SamplesNA12155
Known GenesCHRNA7, GOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
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)essv19612
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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