A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891929



Internal ID18839639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12407946..12414528hg38UCSC Ensembl
Outerchr11:12407829..12415978hg38UCSC Ensembl
Innerchr11:12429493..12436075hg19UCSC Ensembl
Outerchr11:12429376..12437525hg19UCSC Ensembl
Innerchr11:12386069..12392651hg18UCSC Ensembl
Outerchr11:12385952..12394101hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg388150
hg198150
hg188150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797497, essv25797486, essv25800517
Samples
Known GenesPARVA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891929
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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