A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1333n54



Internal ID20134757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87893121..87893929hg38UCSC Ensembl
chr10:89652878..89653686hg19UCSC Ensembl
chr10:89642858..89643666hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38809
hg19809
hg18809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551836, nsv551834, nsv551833, nsv551835
Samples
Known GenesPTEN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1333n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss49
Observed Complex0
Frequencyn/a


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