A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586027



Internal ID7057409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52994359..53007503hg38UCSC Ensembl
Innerchr3:53028375..53041519hg19UCSC Ensembl
Innerchr3:53003415..53016559hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3813145
hg1913145
hg1813145
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991487
Supporting Variants
SamplesHuRef
Known GenesSFMBT1
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586027
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