A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13441



Internal ID9610827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:11679520..11822118hg38UCSC Ensembl
Innerchr6:11679753..11822351hg19UCSC Ensembl
Innerchr6:11787739..11930337hg18UCSC Ensembl
Innerchr6:11787739..11930337hg17UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38142599
hg19142599
hg18142599
hg17142599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758036
Supporting Variants
SamplesNA19192
Known GenesADTRP
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)essv13441
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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