A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3352980



Internal ID15199961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45569626..45571024hg38UCSC Ensembl
Innerchr11:45570024..45570626hg38UCSC Ensembl
Outerchr11:45568626..45572024hg38UCSC Ensembl
chr11:45591176..45592574hg19UCSC Ensembl
Innerchr11:45591574..45592176hg19UCSC Ensembl
Outerchr11:45590176..45593574hg19UCSC Ensembl
chr11:45547752..45549150hg18UCSC Ensembl
Innerchr11:45548752..45548150hg18UCSC Ensembl
Outerchr11:45546752..45550150hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688369
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3352980
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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