A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1217n100



Internal ID20152833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67730549..67893696hg38UCSC Ensembl
chr11:67498020..67661167hg19UCSC Ensembl
chr11:67254596..67417743hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38163148
hg19163148
hg18163148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052828, nsv1045989
Samples
Known GenesFAM86C2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1217n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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