A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760049



Internal ID9635508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84719698..84873299hg38UCSC Ensembl
Innerchr15:85262929..85416530hg19UCSC Ensembl
Innerchr15:83063933..83217534hg18UCSC Ensembl
Innerchr15:83063933..83217534hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38153602
hg19153602
hg18153602
hg17153602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758393
SamplesNA18550
Known GenesALPK3, ZNF592
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)esv2760049
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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