A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1281n100



Internal ID22787368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116101490..116130462hg38UCSC Ensembl
chr11:115972207..116001179hg19UCSC Ensembl
chr11:115477417..115506389hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3828973
hg1928973
hg1828973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045102, nsv1045450
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)dgv1281n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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