A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9033



Internal ID9631122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:53600852..53742885hg38UCSC Ensembl
Innerchr10:55360612..55502645hg19UCSC Ensembl
Innerchr10:55030618..55172651hg18UCSC Ensembl
Innerchr10:55030618..55172651hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38142034
hg19142034
hg18142034
hg17142034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758220
Supporting Variants
SamplesNA19132
Known Genes
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)essv9033
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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