A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865491



Internal ID14646029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62386441..62386485hg38UCSC Ensembl
Innerchr11:62386434..62386492hg38UCSC Ensembl
Outerchr11:62386390..62386536hg38UCSC Ensembl
chr11:62153913..62153957hg19UCSC Ensembl
Innerchr11:62153906..62153964hg19UCSC Ensembl
Outerchr11:62153862..62154008hg19UCSC Ensembl
chr11:61910489..61910533hg18UCSC Ensembl
Innerchr11:61910540..61910482hg18UCSC Ensembl
Outerchr11:61910438..61910584hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3852
hg1952
hg1852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3408585
Supporting Variants
SamplesNA18961
Known GenesASRGL1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865491
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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