A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989065



Internal ID12979638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98898171..98911263hg38UCSC Ensembl
Innerchr11:98768901..98781993hg19UCSC Ensembl
Innerchr11:98274111..98287203hg18UCSC Ensembl
Innerchr11:98274111..98287203hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3813093
hg1913093
hg1813093
hg1713093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35016
Supporting Variants
SamplesNA12891
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989065
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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