A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10520



Internal ID9607582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170272663..170535221hg38UCSC Ensembl
Innerchr6:170581751..170844309hg19UCSC Ensembl
Innerchr6:170423676..170686234hg18UCSC Ensembl
Innerchr6:170499383..170761941hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38262559
hg19262559
hg18262559
hg17262559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758097, esv2758098
Supporting Variants
SamplesNA19240
Known GenesDLL1, FAM120B, FLJ38122, MIR4644, PSMB1
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)essv10520
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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