A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11096



Internal ID9608221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:8123950..8356097hg38UCSC Ensembl
Innerchr12:8276546..8508693hg19UCSC Ensembl
Innerchr12:8167813..8399960hg18UCSC Ensembl
Innerchr12:8167813..8399960hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38232148
hg19232148
hg18232148
hg17232148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758292
Supporting Variants
SamplesNA19211
Known GenesCLEC4A, FAM66C, FAM86FP, FAM90A1, POU5F1P3, ZNF705A
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)essv11096
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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