A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1093n100



Internal ID20152709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33007427..33477800hg38UCSC Ensembl
chr11:33028973..33499346hg19UCSC Ensembl
chr11:32985549..33455922hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38470374
hg19470374
hg18470374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038920, nsv1053344
Samples
Known GenesCSTF3, CSTF3-AS1, DEPDC7, HIPK3, LINC00294, TCP11L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1093n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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