A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1446n54



Internal ID20134870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131112246..131114439hg38UCSC Ensembl
chr10:132910509..132912702hg19UCSC Ensembl
chr10:132800499..132802692hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382194
hg192194
hg182194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552441, nsv552440, nsv552438
Samples
Known GenesTCERG1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1446n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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