A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891804



Internal ID19186200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34513549..34652866hg38UCSC Ensembl
Outerchr2:34492732..34652866hg38UCSC Ensembl
Innerchr2:34738616..34877933hg19UCSC Ensembl
Outerchr2:34717799..34877933hg19UCSC Ensembl
Innerchr2:34592120..34731437hg18UCSC Ensembl
Outerchr2:34571303..34731437hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38160135
hg19160135
hg18160135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797420, essv25797890
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891804
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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