A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161287



Internal ID8252894
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 StatusS
Merged Variantsesv2422367
Supporting Variants
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)essv5161287
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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