A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8651826



Internal ID15099958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69215557..69215720hg38UCSC Ensembl
Innerchr11:69215557..69215720hg38UCSC Ensembl
Outerchr11:69214695..69216249hg38UCSC Ensembl
chr11:68983024..68983187hg19UCSC Ensembl
Innerchr11:68983024..68983187hg19UCSC Ensembl
Outerchr11:68982162..68983716hg19UCSC Ensembl
chr11:68739600..68739763hg18UCSC Ensembl
Innerchr11:68739600..68739763hg18UCSC Ensembl
Outerchr11:68738738..68740292hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38164
hg19164
hg18164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3443839
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8651826
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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