A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10443



Internal ID9607496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30199525..30477791hg38UCSC Ensembl
Innerchr15:30491728..30769994hg19UCSC Ensembl
Innerchr15:28279020..28557286hg18UCSC Ensembl
Innerchr15:28279020..28557286hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38278267
hg19278267
hg18278267
hg17278267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758374
Supporting Variants
SamplesNA18515
Known GenesCHRFAM7A, DKFZP434L187, LOC101059918
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)essv10443
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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