A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1218n100



Internal ID20152834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67730549..67942321hg38UCSC Ensembl
chr11:67498020..67709792hg19UCSC Ensembl
chr11:67254596..67466368hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38211773
hg19211773
hg18211773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048996, nsv1053863, nsv1039130, nsv1039721, nsv1036397, nsv1053095, nsv1036003
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)dgv1218n100
Frequency
Sample Size29084
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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