A curated catalogue of human genomic structural variation




Variant Details

Variant: essv24039



Internal ID9622602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34306400..34590436hg38UCSC Ensembl
Innerchr15:34598601..34882637hg19UCSC Ensembl
Innerchr15:32385893..32669929hg18UCSC Ensembl
Innerchr15:32385893..32669929hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38284037
hg19284037
hg18284037
hg17284037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758376
Supporting Variants
SamplesNA10859
Known GenesGOLGA8A, GOLGA8B, LPCAT4, MIR1233-1, MIR1233-2, NOP10, NUTM1, SLC12A6
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)essv24039
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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