A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156346



Internal ID22084822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:54392935..54399485hg38UCSC Ensembl
Outerchr5:54391815..54400729hg38UCSC Ensembl
Innerchr5:53688765..53695315hg19UCSC Ensembl
Outerchr5:53687645..53696559hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg388915
hg198915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv230n97
Supporting Variantsnssv4017546
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156346
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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