A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422440



Internal ID7906537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25850790..25988300hg38UCSC Ensembl
Innerchr9:25850788..25988298hg19UCSC Ensembl
Innerchr9:25840788..25978298hg18UCSC Ensembl
Innerchr9:25840788..25978298hg17UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38137511
hg19137511
hg18137511
hg17137511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161380
SamplesND01684
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422440
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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