A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757859



Internal ID9633318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14869763..15121196hg38UCSC Ensembl
Innerchr3:14911270..15162703hg19UCSC Ensembl
Innerchr3:14886274..15137707hg18UCSC Ensembl
Innerchr3:14886274..15137707hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38251434
hg19251434
hg18251434
hg17251434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759130
Supporting Variantsessv22874
SamplesNA12760
Known GenesFGD5, FGD5-AS1, MRPS25, NR2C2, ZFYVE20
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)esv2757859
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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