A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759652



Internal ID9635111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144300010..144472295hg38UCSC Ensembl
Innerchr8:145523693..145697678hg19UCSC Ensembl
Innerchr8:145494501..145668486hg18UCSC Ensembl
Innerchr8:145494501..145668486hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38172286
hg19173986
hg18173986
hg17173986
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758625
SamplesNA19005, NA18540
Known GenesADCK5, CPSF1, CYHR1, DGAT1, FBXL6, HSF1, KIFC2, LOC100287098, MIR1234, MIR6848, MIR6849, MIR6893, MIR939, SCRT1, SLC39A4, SLC52A2, TMEM249, TONSL, VPS28
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)esv2759652
Frequency
Sample Size270
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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