A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586059



Internal ID7057441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32464140..32464800hg38UCSC Ensembl
Innerchr6:32431917..32432577hg19UCSC Ensembl
Innerchr6:32539895..32540555hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38661
hg19661
hg18661
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989366
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586059
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