A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv26e196



Internal ID20123225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162102803..162384768hg38UCSC Ensembl
chr6:162523835..162805800hg19UCSC Ensembl
chr6:162443825..162725790hg18UCSC Ensembl
chr6:162494246..162776211hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38281966
hg19281966
hg18281966
hg17281966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2422322, esv2422334, esv2422289
SamplesND04788, ND05093, ND01583
Known GenesPARK2
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)dgv26e196
Frequency
Sample Size181
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer