A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1105n54



Internal ID20134529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44753495..44864035hg38UCSC Ensembl
chr10:45248943..45359483hg19UCSC Ensembl
chr10:44568949..44679489hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38110541
hg19110541
hg18110541
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550712, nsv550713
Samples
Known GenesTMEM72-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1105n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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