A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14287905



Internal ID1022829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112393016..112396620hg38UCSC Ensembl
Innerchr11:112393066..112396570hg38UCSC Ensembl
Outerchr11:112392966..112396670hg38UCSC Ensembl
chr11:112263739..112267343hg19UCSC Ensembl
Innerchr11:112263789..112267293hg19UCSC Ensembl
Outerchr11:112263689..112267393hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383605
hg193605
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627755
Supporting Variants
SamplesHG00640
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14287905
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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