A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1058n100



Internal ID19011426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11881285..11953953hg38UCSC Ensembl
chr11:11902832..11975500hg19UCSC Ensembl
chr11:11859408..11932076hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3872669
hg1972669
hg1872669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046928, nsv1054274
Samples
Known GenesUSP47
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1058n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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