A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7743275



Internal ID14440358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45893260..45893261hg38UCSC Ensembl
Innerchr11:45893234..45893287hg38UCSC Ensembl
Outerchr11:45893233..45893288hg38UCSC Ensembl
chr11:45914811..45914812hg19UCSC Ensembl
Innerchr11:45914785..45914838hg19UCSC Ensembl
Outerchr11:45914784..45914839hg19UCSC Ensembl
chr11:45871387..45871388hg18UCSC Ensembl
Innerchr11:45871414..45871361hg18UCSC Ensembl
Outerchr11:45871360..45871415hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38155
hg19155
hg18155
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3304212
Supporting Variants
SamplesNA18916
Known GenesMAPK8IP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7743275
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