A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006184



Internal ID7071277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:21719678..21723052hg38UCSC Ensembl
Outerchr19:21902480..21905854hg19UCSC Ensembl
Outerchr19:21694320..21697694hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg383375
hg193375
hg183375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564327
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006184
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