A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891906



Internal ID19186302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:336332..366710hg38UCSC Ensembl
Outerchr11:336332..366710hg38UCSC Ensembl
Innerchr11:336332..366710hg19UCSC Ensembl
Outerchr11:336332..366710hg19UCSC Ensembl
Innerchr11:326332..356710hg18UCSC Ensembl
Outerchr11:326332..356710hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3830379
hg1930379
hg1830379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783308
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891906
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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