A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3397620



Internal ID15244583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67583387..67583387hg38UCSC Ensembl
Innerchr11:67583386..67583388hg38UCSC Ensembl
Outerchr11:67583327..67583437hg38UCSC Ensembl
chr11:67350858..67350858hg19UCSC Ensembl
Innerchr11:67350857..67350859hg19UCSC Ensembl
Outerchr11:67350798..67350908hg19UCSC Ensembl
chr11:67107434..67107434hg18UCSC Ensembl
Innerchr11:67107435..67107433hg18UCSC Ensembl
Outerchr11:67107374..67107484hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8812637
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3397620
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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