A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9908



Internal ID9632093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1496135..1611612hg38UCSC Ensembl
Innerchr20:1476781..1592258hg19UCSC Ensembl
Innerchr20:1424781..1540258hg18UCSC Ensembl
Innerchr20:1424781..1540258hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38115478
hg19115478
hg18115478
hg17115478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758509
Supporting Variants
SamplesNA19145
Known GenesSIRPB1, SIRPD
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)essv9908
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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