A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17294



Internal ID9615107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143773822..144210439hg38UCSC Ensembl
Innerchr4:144694975..145131592hg19UCSC Ensembl
Innerchr4:144914425..145351042hg18UCSC Ensembl
Innerchr4:145052580..145489197hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38436618
hg19436618
hg18436618
hg17436618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757960
Supporting Variants
SamplesNA18856
Known GenesGYPA, GYPB, GYPE
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)essv17294
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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