A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6920



Internal ID9965360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13804558..13967431hg38UCSC Ensembl
Innerchr21:15176879..15339752hg19UCSC Ensembl
Innerchr21:14098750..14261623hg18UCSC Ensembl
Innerchr21:14098750..14261623hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38162874
hg19162874
hg18162874
hg17162874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758529
Supporting Variants
SamplesNA18605
Known GenesANKRD20A11P, C21orf15
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)essv6920
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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