A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422404



Internal ID7906501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:899186..1406833hg38UCSC Ensembl
Innerchr3:940869..1448517hg19UCSC Ensembl
Innerchr3:915869..1423517hg18UCSC Ensembl
Innerchr3:915869..1423517hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38507648
hg19507649
hg18507649
hg17507649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161522
SamplesND03627
Known GenesCNTN6
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422404
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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