A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1208n100



Internal ID20152824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59023509..59097071hg38UCSC Ensembl
chr11:58790982..58864544hg19UCSC Ensembl
chr11:58547558..58621120hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3873563
hg1973563
hg1873563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053361, nsv1039379, nsv1052514, nsv1049182, nsv1047758, nsv1050297, nsv1050767
Samples
Known GenesLOC283194
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1208n100
Frequency
Sample Size29084
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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