A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13735



Internal ID9611153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3215282..3398350hg38UCSC Ensembl
Innerchr11:3236512..3419580hg19UCSC Ensembl
Innerchr11:3193088..3376156hg18UCSC Ensembl
Innerchr11:3193088..3376156hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38183069
hg19183069
hg18183069
hg17183069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758252
Supporting Variants
SamplesNA19119
Known GenesLOC650368, MRGPRE, MRGPRG, MRGPRG-AS1, OR7E12P, ZNF195
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)essv13735
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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