A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422449



Internal ID7906546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31069845..31122236hg38UCSC Ensembl
Innerchr12:31222779..31275170hg19UCSC Ensembl
Innerchr12:31114046..31166437hg18UCSC Ensembl
Innerchr12:31114046..31166437hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3852392
hg1952392
hg1852392
hg1752392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8e196
Supporting Variantsessv5161397
SamplesND03633
Known GenesDDX11, DDX11-AS1
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422449
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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