A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740710



Internal ID15082780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10795835..10795835hg38UCSC Ensembl
Innerchr11:10795834..10795836hg38UCSC Ensembl
Outerchr11:10795785..10795885hg38UCSC Ensembl
chr11:10817382..10817382hg19UCSC Ensembl
Innerchr11:10817381..10817383hg19UCSC Ensembl
Outerchr11:10817332..10817432hg19UCSC Ensembl
chr11:10773958..10773958hg18UCSC Ensembl
Innerchr11:10773959..10773957hg18UCSC Ensembl
Outerchr11:10773908..10774008hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381764
hg191764
hg181764
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3353329
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740710
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