A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422367



Internal ID8253150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25118501..25214174hg38UCSC Ensembl
Innerchr9:25118499..25214172hg19UCSC Ensembl
Innerchr9:25108499..25204172hg18UCSC Ensembl
Innerchr9:25108499..25204172hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3895674
hg1995674
hg1895674
hg1795674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv32e196
Supporting Variantsessv5161287
SamplesND04404
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422367
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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