A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3415573



Internal ID15262532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68963594..68964217hg38UCSC Ensembl
Innerchr11:68963594..68964217hg38UCSC Ensembl
Outerchr11:68961731..68964739hg38UCSC Ensembl
chr11:68731063..68731686hg19UCSC Ensembl
Innerchr11:68731063..68731686hg19UCSC Ensembl
Outerchr11:68729200..68732208hg19UCSC Ensembl
chr11:68487639..68488262hg18UCSC Ensembl
Innerchr11:68487639..68488262hg18UCSC Ensembl
Outerchr11:68485776..68488784hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38624
hg19624
hg18624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8651825
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3415573
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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