A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10689



Internal ID9607768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87193550..87550005hg38UCSC Ensembl
Innerchr10:88953307..89309762hg19UCSC Ensembl
Innerchr10:88943287..89299742hg18UCSC Ensembl
Innerchr10:88943287..89299742hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38356456
hg19356456
hg18356456
hg17356456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758234
Supporting Variants
SamplesNA18855
Known GenesLINC00864, LOC439994, MINPP1, MIR4678, 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)essv10689
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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