A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155648



Internal ID22086153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15287076..15321728hg38UCSC Ensembl
Outerchr20:15275497..15324612hg38UCSC Ensembl
Innerchr20:15267722..15302374hg19UCSC Ensembl
Outerchr20:15256143..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 Variantsdgv179n97
Supporting Variantsnssv4013879
Samples
Known GenesMACROD2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155648
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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