A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1134n54



Internal ID20134558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52051671..52081345hg38UCSC Ensembl
chr10:53811431..53841105hg19UCSC Ensembl
chr10:53481437..53511111hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3829675
hg1929675
hg1829675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550874, nsv550873
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1134n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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