A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3366851



Internal ID15213827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110031666..110031744hg38UCSC Ensembl
Innerchr6:110031689..110031721hg38UCSC Ensembl
Outerchr6:110031643..110031767hg38UCSC Ensembl
chr6:110352869..110352947hg19UCSC Ensembl
Innerchr6:110352892..110352924hg19UCSC Ensembl
Outerchr6:110352846..110352970hg19UCSC Ensembl
chr6:110459562..110459640hg18UCSC Ensembl
Innerchr6:110459585..110459617hg18UCSC Ensembl
Outerchr6:110459539..110459663hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3879
hg1979
hg1879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8671321, essv8671322
SamplesNA19238, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3366851
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer