A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1286n100



Internal ID22787373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119901039..119938155hg38UCSC Ensembl
chr11:119771748..119808864hg19UCSC Ensembl
chr11:119276958..119314074hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3837117
hg1937117
hg1837117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048084, nsv1049086
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)dgv1286n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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