A curated catalogue of human genomic structural variation




Variant Details

Variant: essv22409



Internal ID9956303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30000741..30566283hg38UCSC Ensembl
Innerchr15:30292944..30858486hg19UCSC Ensembl
Innerchr15:28080236..28645778hg18UCSC Ensembl
Innerchr15:28080236..28645778hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38565543
hg19565543
hg18565543
hg17565543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758374
Supporting Variants
SamplesNA10861
Known GenesCHRFAM7A, DKFZP434L187, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3
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)essv22409
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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