A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003583



Internal ID7068688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:1948212..1959035hg38UCSC Ensembl
Outerchr16:1998213..2009036hg19UCSC Ensembl
Outerchr16:1938214..1949037hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3810824
hg1910824
hg1810824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565731
SamplesHuRef
Known GenesRPL3L
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003583
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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