A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587105



Internal ID7058487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:125963769..125964265hg38UCSC Ensembl
Innerchr12:126448315..126448811hg19UCSC Ensembl
Innerchr12:125014268..125014764hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38497
hg19497
hg18497
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1007158
Supporting Variants
SamplesHuRef
Known GenesLINC00939
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587105
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