A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv179n97



Internal ID22815576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:15275497..15324612hg38UCSC Ensembl
chr20:15256143..15305258hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3849116
hg1949116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155649, nsv1155648
Samples
Known GenesMACROD2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv179n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer