A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1108n100



Internal ID22787195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42876382..42949618hg38UCSC Ensembl
chr11:42897932..42971168hg19UCSC Ensembl
chr11:42854508..42927744hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3873237
hg1973237
hg1873237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039362, nsv1048037, nsv1035450
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1108n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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