A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565169



Internal ID7036551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:50897888..50899995hg38UCSC Ensembl
Outerchr19:51401144..51403251hg19UCSC Ensembl
Outerchr19:56092956..56095063hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382108
hg192108
hg182108
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1010378
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565169
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