A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2806n100



Internal ID19013174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21552771..21759413hg38UCSC Ensembl
chr16:21564092..21770734hg19UCSC Ensembl
chr16:21471593..21678235hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38206643
hg19206643
hg18206643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044947, nsv1035287, nsv1048102, nsv1048779, nsv1054842
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2806n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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