A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154912



Internal ID22085417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61139335..61144209hg38UCSC Ensembl
Outerchr13:61137182..61152762hg38UCSC Ensembl
Innerchr13:61713469..61718343hg19UCSC Ensembl
Outerchr13:61711316..61726896hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3815581
hg1915581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008144
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154912
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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