A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996812



Internal ID7080782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:89969484..89979238hg38UCSC Ensembl
Outerchr15:90512716..90522470hg19UCSC Ensembl
Outerchr15:88313720..88323474hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg389755
hg199755
hg189755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564388
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996812
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