A curated catalogue of human genomic structural variation




Variant Details

Variant: essv21777



Internal ID9958799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20397790..20609679hg38UCSC Ensembl
Innerchr10:20686719..20898608hg19UCSC Ensembl
Innerchr10:20726725..20938614hg18UCSC Ensembl
Innerchr10:20726725..20938614hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38211890
hg19211890
hg18211890
hg17211890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758212
Supporting Variants
SamplesNA12239
Known GenesMIR4675
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)essv21777
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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