A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891946



Internal ID19186342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21843050..21989175hg38UCSC Ensembl
Outerchr11:21819660..22101567hg38UCSC Ensembl
Innerchr11:21864596..22010721hg19UCSC Ensembl
Outerchr11:21841206..22123113hg19UCSC Ensembl
Innerchr11:21821172..21967297hg18UCSC Ensembl
Outerchr11:21797782..22079689hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38281908
hg19281908
hg18281908
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797119, essv25785199, essv25791408, essv25796210, essv25781503, essv25780283
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891946
Frequency
Sample Size3017
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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