A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11066n54



Internal ID22778961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168316348..168317914hg38UCSC Ensembl
chr6:168717028..168718594hg19UCSC Ensembl
chr6:168459877..168461443hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381567
hg191567
hg181567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605468, nsv605465, nsv605461
Samples
Known GenesDACT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11066n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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