A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3416893



Internal ID15263851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3173346..3175244hg38UCSC Ensembl
Innerchr11:3174244..3174346hg38UCSC Ensembl
Outerchr11:3172346..3176244hg38UCSC Ensembl
chr11:3194576..3196474hg19UCSC Ensembl
Innerchr11:3195474..3195576hg19UCSC Ensembl
Outerchr11:3193576..3197474hg19UCSC Ensembl
chr11:3151152..3153050hg18UCSC Ensembl
Innerchr11:3152152..3152050hg18UCSC Ensembl
Outerchr11:3150152..3154050hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381899
hg191899
hg181899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv553e59
Supporting Variantsessv8688260
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3416893
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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