A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11009



Internal ID9608125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86965868..87445609hg38UCSC Ensembl
Innerchr10:88725625..89205366hg19UCSC Ensembl
Innerchr10:88715605..89195346hg18UCSC Ensembl
Innerchr10:88715605..89195346hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38479742
hg19479742
hg18479742
hg17479742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758234
Supporting Variants
SamplesNA19143
Known GenesADIRF, AGAP11, FAM25A, FAM35A, GLUD1, LINC00864, LOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
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)essv11009
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer