A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1213n100



Internal ID22787300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61987149..62108238hg38UCSC Ensembl
chr11:61754621..61875710hg19UCSC Ensembl
chr11:61511197..61632286hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38121090
hg19121090
hg18121090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054452, nsv1053479, nsv1035515
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)dgv1213n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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