A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1116n54



Internal ID18993292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46224041..46306785hg38UCSC Ensembl
chr10:47595277..47678021hg19UCSC Ensembl
chr10:47065283..47148027hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3882745
hg1982745
hg1882745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550777, nsv550779, nsv550778
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1116n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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