A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6187n100



Internal ID20157803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162404070..162594675hg38UCSC Ensembl
chr6:162825102..163015707hg19UCSC Ensembl
chr6:162745092..162935697hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38190606
hg19190606
hg18190606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034495, nsv1021711
Samples
Known GenesPARK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6187n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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