A curated catalogue of human genomic structural variation




Variant Details

Variant: essv22044



Internal ID9620386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30000741..30726259hg38UCSC Ensembl
Innerchr15:30292944..31018462hg19UCSC Ensembl
Innerchr15:28080236..28805754hg18UCSC Ensembl
Innerchr15:28080236..28805754hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38725519
hg19725519
hg18725519
hg17725519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758374
Supporting Variants
SamplesNA12154
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)essv22044
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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