A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2757894



Internal ID9633353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143273855..143567137hg38UCSC Ensembl
Innerchr3:142992697..143285979hg19UCSC Ensembl
Innerchr3:144475387..144768669hg18UCSC Ensembl
Innerchr3:144475395..144768677hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38293283
hg19293283
hg18293283
hg17293283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2759184
Supporting Variantsessv21217
SamplesNA11830
Known GenesSLC9A9, SLC9A9-AS1
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)esv2757894
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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