A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8956



Internal ID9631035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60001..146701hg38UCSC Ensembl
Innerchr6:60001..146701hg19UCSC Ensembl
Innerchr6:5001..91701hg18UCSC Ensembl
Innerchr6:5001..91701hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3886701
hg1986701
hg1886701
hg1786701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758034
Supporting Variants
SamplesNA19200
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)essv8956
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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