A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759764



Internal ID9635223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68697962..68871556hg38UCSC Ensembl
Innerchr10:70457719..70631312hg19UCSC Ensembl
Innerchr10:70127725..70301318hg18UCSC Ensembl
Innerchr10:70127725..70301318hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38173595
hg19173594
hg18173594
hg17173594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758227
SamplesNA19161, NA18853, NA18523
Known GenesCCAR1, SNORD98, STOX1
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)esv2759764
Frequency
Sample Size270
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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