A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563655



Internal ID7036415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:91519903..91529383hg38UCSC Ensembl
Outerchr8:92532131..92541611hg19UCSC Ensembl
Outerchr8:92601307..92610787hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg389481
hg199481
hg189481
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv993266
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563655
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