A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161235



Internal ID7905949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1855887..2813527hg38UCSC Ensembl
Innerchr3:1897571..2855211hg19UCSC Ensembl
Innerchr3:1872571..2830211hg18UCSC Ensembl
Innerchr3:1872571..2830211hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38957641
hg19957641
hg18957641
hg17957641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422325
Supporting Variants
SamplesND04675
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161235
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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