A curated catalogue of human genomic structural variation




Variant Details

Variant: essv23686



Internal ID9956351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165728153..165885447hg38UCSC Ensembl
Innerchr6:166141641..166298935hg19UCSC Ensembl
Innerchr6:166061631..166218925hg18UCSC Ensembl
Innerchr6:166112052..166269346hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38157295
hg19157295
hg18157295
hg17157295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758093
Supporting Variants
SamplesNA10863
Known Genes
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)essv23686
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