A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1109n100



Internal ID20152725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43925389..43947681hg38UCSC Ensembl
chr11:43946939..43969231hg19UCSC Ensembl
chr11:43903515..43925807hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3822293
hg1922293
hg1822293
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040880, nsv1039292
Samples
Known GenesC11orf96
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1109n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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