A curated catalogue of human genomic structural variation




Variant Details

Variant: essv20430



Internal ID9618593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30000741..30655412hg38UCSC Ensembl
Innerchr15:30292944..30947615hg19UCSC Ensembl
Innerchr15:28080236..28734907hg18UCSC Ensembl
Innerchr15:28080236..28734907hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38654672
hg19654672
hg18654672
hg17654672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758374
Supporting Variants
SamplesNA10830
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC100288637, 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)essv20430
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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