A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3398560



Internal ID15245523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3653646..3654844hg38UCSC Ensembl
Innerchr11:3653844..3654646hg38UCSC Ensembl
Outerchr11:3652646..3655844hg38UCSC Ensembl
chr11:3674876..3676074hg19UCSC Ensembl
Innerchr11:3675074..3675876hg19UCSC Ensembl
Outerchr11:3673876..3677074hg19UCSC Ensembl
chr11:3631452..3632650hg18UCSC Ensembl
Innerchr11:3632452..3631650hg18UCSC Ensembl
Outerchr11:3630452..3633650hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv555e59
Supporting Variantsessv8688274
SamplesNA19240
Known GenesART1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3398560
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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