A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2759490



Internal ID9634949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163571032..163740871hg38UCSC Ensembl
Innerchr6:163992064..164161903hg19UCSC Ensembl
Innerchr6:163912054..164081893hg18UCSC Ensembl
Innerchr6:163962475..164132314hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38169840
hg19169840
hg18169840
hg17169840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2758092
SamplesNA12874
Known GenesQKI
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)esv2759490
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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