A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12740n54



Internal ID20146164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69126301..69128184hg38UCSC Ensembl
chr9:71741217..71743100hg19UCSC Ensembl
chr9:70931037..70932920hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381884
hg191884
hg181884
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614556, nsv614558
Samples
Known GenesTJP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12740n54
Frequency
Sample Size17421
Observed Gain27
Observed Loss1005
Observed Complex0
Frequencyn/a


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