A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3551721



Internal ID18752797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70611901..70612015hg38UCSC Ensembl
Outerchr14:70611881..70612039hg38UCSC Ensembl
Innerchr14:71078618..71078732hg19UCSC Ensembl
Outerchr14:71078598..71078756hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9750468
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3551721
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