A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891945



Internal ID19186341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21716803..21774732hg38UCSC Ensembl
Outerchr11:21716803..21774732hg38UCSC Ensembl
Innerchr11:21738349..21796278hg19UCSC Ensembl
Outerchr11:21738349..21796278hg19UCSC Ensembl
Innerchr11:21694925..21752854hg18UCSC Ensembl
Outerchr11:21694925..21752854hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3857930
hg1957930
hg1857930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796627
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891945
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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