A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586381



Internal ID6711077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:165158182..165171586hg38UCSC Ensembl
Innerchr2:166014692..166028096hg19UCSC Ensembl
Innerchr2:165722938..165736342hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3813405
hg1913405
hg1813405
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992100
Supporting Variants
SamplesHuRef
Known GenesSCN3A
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586381
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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