A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586864



Internal ID7058246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99909957..99910760hg38UCSC Ensembl
Innerchr3:99628801..99629604hg19UCSC Ensembl
Innerchr3:101111491..101112294hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38804
hg19804
hg18804
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998785
Supporting Variants
SamplesHuRef
Known GenesCMSS1, FILIP1L, MIR548G
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586864
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