A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586927



Internal ID7058309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:237012160..237012610hg38UCSC Ensembl
Innerchr2:237920803..237921253hg19UCSC Ensembl
Innerchr2:237585542..237585992hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38451
hg19451
hg18451
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995424
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586927
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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