A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv31e196



Internal ID22757701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:136527277..136735750hg38UCSC Ensembl
chr8:137539520..137747993hg19UCSC Ensembl
chr8:137608702..137817175hg18UCSC Ensembl
chr8:137608702..137817175hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38208474
hg19208474
hg18208474
hg17208474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2422462, esv2422411
SamplesND01885, ND01688
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)dgv31e196
Frequency
Sample Size181
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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