A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2760064



Internal ID9635523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101731427..101890871hg38UCSC Ensembl
Innerchr15:102271630..102431074hg19UCSC Ensembl
Innerchr15:100089153..100248597hg18UCSC Ensembl
Innerchr15:100089153..100248597hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38159445
hg19159445
hg18159445
hg17159445
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758404
SamplesNA10831
Known GenesOR4F13P, OR4F15, OR4F6
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)esv2760064
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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