A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3551560



Internal ID18752636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:52127968..52128260hg38UCSC Ensembl
Outerchr14:52127899..52128298hg38UCSC Ensembl
Innerchr14:52594686..52594978hg19UCSC Ensembl
Outerchr14:52594617..52595016hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750307
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3551560
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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