A curated catalogue of human genomic structural variation




Variant Details

Variant: essv17477



Internal ID9615310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:36996835..37336771hg38UCSC Ensembl
Innerchr10:37285763..37625699hg19UCSC Ensembl
Innerchr10:37325769..37665705hg18UCSC Ensembl
Innerchr10:37325769..37665705hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38339937
hg19339937
hg18339937
hg17339937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758213
Supporting Variants
SamplesNA12762
Known GenesANKRD30A, LINC00993
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)essv17477
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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