A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8806



Internal ID9630869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16091360..16303255hg38UCSC Ensembl
Innerchr16:16185217..16397112hg19UCSC Ensembl
Innerchr16:16092718..16304613hg18UCSC Ensembl
Innerchr16:16092718..16304613hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38211896
hg19211896
hg18211896
hg17211896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758412
Supporting Variants
SamplesNA18508
Known GenesABCC1, ABCC6, MIR3179-1, MIR3179-2, MIR3179-3, NOMO3
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)essv8806
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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