A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3412508



Internal ID15259467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61022884..61022903hg38UCSC Ensembl
Innerchr11:61022880..61022907hg38UCSC Ensembl
Outerchr11:61022861..61022926hg38UCSC Ensembl
chr11:60790356..60790375hg19UCSC Ensembl
Innerchr11:60790352..60790379hg19UCSC Ensembl
Outerchr11:60790333..60790398hg19UCSC Ensembl
chr11:60546932..60546951hg18UCSC Ensembl
Innerchr11:60546955..60546928hg18UCSC Ensembl
Outerchr11:60546909..60546974hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9652758
SamplesNA12814
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3412508
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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