A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16252



Internal ID9613950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32327966..32529598hg38UCSC Ensembl
Innerchr15:32620167..32821799hg19UCSC Ensembl
Innerchr15:30407459..30609091hg18UCSC Ensembl
Innerchr15:30407459..30609091hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38201633
hg19201633
hg18201633
hg17201633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758375
Supporting Variants
SamplesNA19161
Known GenesGOLGA8K, 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)essv16252
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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