A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1239n100



Internal ID22787326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80261889..80278911hg38UCSC Ensembl
chr11:79972933..79989955hg19UCSC Ensembl
chr11:79650581..79667603hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3817023
hg1917023
hg1817023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052132, nsv1037876
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)dgv1239n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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