A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005485



Internal ID7070580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95621242..95622546hg38UCSC Ensembl
Innerchr14:96087579..96088883hg19UCSC Ensembl
Innerchr14:95157332..95158636hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg381305
hg191305
hg181305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586925
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005485
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer