A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1301n100



Internal ID20152917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133922841..133959811hg38UCSC Ensembl
chr11:133792736..133829706hg19UCSC Ensembl
chr11:133297946..133334916hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3836971
hg1936971
hg1836971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052225, nsv1045123, nsv1041531, nsv1039760, nsv1044409, nsv1046642, nsv1043506
Samples
Known GenesIGSF9B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1301n100
Frequency
Sample Size29084
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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