A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422265



Internal ID7906362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17396713..17598189hg38UCSC Ensembl
Innerchr9:17396711..17598187hg19UCSC Ensembl
Innerchr9:17386711..17588187hg18UCSC Ensembl
Innerchr9:17386711..17588187hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38201477
hg19201477
hg18201477
hg17201477
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161298
SamplesND03903
Known GenesCNTLN, SH3GL2
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422265
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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