A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3553907



Internal ID18408297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89587762..89588160hg38UCSC Ensembl
Outerchr16:89587642..89588234hg38UCSC Ensembl
Innerchr16:89654170..89654568hg19UCSC Ensembl
Outerchr16:89654050..89654642hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9752654
Samples
Known GenesCPNE7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3553907
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